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(1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptane

CAS No.
113451-59-5
Chemical Name:
(1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptane
Synonyms
EOS-61878;(1S,4S)-5-Boc-2,5-diazabicyclo[2.2.1]heptane;(1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptane;(1S,4S)-N-BOC-2,5-DIAZA-BICYCLO[2.2.1]HEPTANE;(1S,4S)-2-T-BOC-2,5-DIAZABICYCLO[2.2.1]HEPTANE;(1S,4S)-(-)-2-BOC-2,5-DIAZABICYCLO[2.2.1]HEPTANE;(1S,4S)-2-N-T-BOC-2,5-DIAZABICYCLO[2.2.1]HEPTANE;(1S,4S)-2-Boc-2,5-diazabicyclo2.2.1üheptane, 97%;(1S,4S)-2,5-Diazabicyclo(2,2,1)Heptane-2-Carboxylate;(1S,4S)-(-)-2-BOC-2,5-diazabicyclo[2.2.1]heptane,95%
CBNumber:
CB7158599
Molecular Formula:
C10H18N2O2
Molecular Weight:
198.26
MDL Number:
MFCD01569250
MOL File:
113451-59-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:54:40

(1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptane Properties

Melting point 74-76 °C(lit.)
alpha -44o (C=1 IN CHLOROFORM)
Boiling point 276.4±15.0 °C(Predicted)
Density 1.104±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Powder
pka 9.74±0.20(Predicted)
color White to slightly beige
optical activity [α]22/D 44°, c = 1 in chloroform
Water Solubility Insoluble in water.
Sensitive Air Sensitive
BRN 6460311
InChI InChI=1S/C10H18N2O2/c1-10(2,3)14-9(13)12-6-7-4-8(12)5-11-7/h7-8,11H,4-6H2,1-3H3/t7-,8-/m0/s1
InChIKey UXAWXZDXVOYLII-YUMQZZPRSA-N
SMILES [C@]12([H])C[C@]([H])(NC1)CN2C(OC(C)(C)C)=O
CAS DataBase Reference 113451-59-5(CAS DataBase Reference)
UNSPSC Code 12352005
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P280-P305+P351+P338-P309-P310
Risk Statements  34
Safety Statements  22-24/25-45-36/37/39-26
RIDADR  3263
WGK Germany  3
HS Code  29335990
Storage Class 11 - Combustible Solids
NFPA 704
1
2 0

(1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptane price More Price(68)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 473049 (1S,4S)-(?)-2-Boc-2,5-diazabicyclo[2.2.1]heptane 95% 113451-59-5 1g $198 2026-04-30 Buy
Sigma-Aldrich 473049 (1S,4S)-(?)-2-Boc-2,5-diazabicyclo[2.2.1]heptane 95% 113451-59-5 5g $559 2026-04-30 Buy
TCI Chemical D6152 tert-Butyl (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane-2-carboxylate min. 98.0 % 113451-59-5 1G $77 2026-04-30 Buy
Usbiological 261699 (1S,4S)-N-Boc-2,5-diazabicyclo[2.2.1]heptane ≥98% 113451-59-5 1g $355 2026-06-03 Buy
Usbiological 261699 (1S,4S)-N-Boc-2,5-diazabicyclo[2.2.1]heptane ≥98% 113451-59-5 5g $708 2026-06-03 Buy
Product number Packaging Price Buy
473049 1g $198 Buy
473049 5g $559 Buy
D6152 1G $77 Buy
261699 1g $355 Buy
261699 5g $708 Buy

(1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptane Chemical Properties, Uses, Production

Chemical Properties

White to slightly beige powder

Uses

It is used as an active pharmaceutical intermediate.

Synthesis

1-Pyrrolidinecarboxylic acid, 2-(azidomethyl)-4-[(methylsulfonyl)oxy]-, 1,1-dimethylethyl ester, (2S,4R)-

113451-54-0

(1S,4S)-2-BOC-2,5-DIAZABICYCLO[2.2.1]HEPTANE

113451-59-5

Methylsulfonate 17 (1.2 g, 3.78 mmol) was used as raw material, which was suspended in anhydrous THF (38 mL), triphenylphosphine (1.48 g, 5.66 mmol) was added, and the reaction was stirred at room temperature for 2 hours. Subsequently, H2O (0.5 mL) was added and stirring was continued for 18 hours. Upon completion of the reaction, the solvent was removed under reduced pressure and the residue was suspended in 1 M hydrochloric acid (150 mL) and extracted with CH2Cl2 (2 x 70 mL). The aqueous layer was adjusted to pH 14 with base and then extracted with CH2Cl2 (3 × 70 mL). The organic phases were combined, washed with brine (100 mL), dried over anhydrous MgSO4 and concentrated under reduced pressure. Purification by rapid chromatography on silica gel with the eluent CH2Cl2-methanol-ammonia (90:9:1) afforded the target product amine 18 (0.52 g, 2.62 mmol, 71% yield) as a colorless solid. The product characterization data were as follows: melting point 76.8-77.9 °C; specific spin [α]D -47.6 (c 1.0, CHCl3); IR spectra (νmax/cm-1) 2975, 1688, 1408, 1170; 1H NMR (500 MHz, CDCl3) δ 4.43 (0.5H, s), 4.30 (0.5H, s), 3.69 (1H, s), 3.38-3.32 (1H, m), 3.19-3.13 (1H, m), 3.06-2.97 (2H, m), 1.75-1.65 (2H, m), 1.45-1.43 (9H, m); 13C NMR (125 MHz, CDCl3) δ 154.6, 154.3, 79.6, 79.5, 57.3, 56.6, 56.5, 56.3, 56.1, 52.8, 52.7, 37.2, 37.0, 28.66; mass spectra (APCI) m/z 199 ([M+H]+, 100).

References

[1] Journal of Organic Chemistry, 1988, vol. 53, # 7, p. 1580 - 1582
[2] Tetrahedron Letters, 2013, vol. 54, # 39, p. 5345 - 5347

Global Suppliers ( 230)
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View Latest Price from (1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptane manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
(1S,4S)-()-2-Boc-2,5-diazabicyclo[2.2.1]heptane pictures 2021-07-02 (1S,4S)-()-2-Boc-2,5-diazabicyclo[2.2.1]heptane
113451-59-5
$10.00-15.00 1KG 99%+ HPLC Zhuozhou Wenxi import and Export Co., Ltd
(1S,4S)-2-BOC-2,5-DIAZABICYCLO[2.2.1]HEPTANE pictures 2019-07-06 (1S,4S)-2-BOC-2,5-DIAZABICYCLO[2.2.1]HEPTANE
113451-59-5
$1.00 1kg 98%min 500kg Career Henan Chemical Co
TERT-BUTYL (1S, 4S)-(-)-2,5-DIAZABICYCLO[2.2.1]HEPTANE-2-CARBOXYLATE TERT-BUTYL (1S,4S)-2,5-DIAZABICYCLO(2.2.1)HEPTANE-2-CARBOXYLATE (1S,4S)-N-(TERT-BUTOXYCARBONYL)-2,5-DIAZABICYCLO[2.2.1]HEPTANE (1S,4S)-(-)-2-BOC-2,5-DIAZABICYCLO[2.2.1]HEPTANE (1S,4S)-2-T-BOC-2,5-DIAZABICYCLO[2.2.1]HEPTANE (1S,4S)-2-N-T-BOC-2,5-DIAZABICYCLO[2.2.1]HEPTANE (1S,4S)-N-BOC-2,5-DIAZA-BICYCLO[2.2.1]HEPTANE N-(tert-Butoxycarbonyl)-2,5-diazabicyclo[2.2.1]heptane~tert-Butyl (1S,4S)-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate (1S,4S)-2,5-Diazabicyclo(2,2,1)Heptane-2-Carboxylate (1R,4R)-2-N-t-BOC-2,5-Diazabicyclo[2.2.1]heptane HBr 1,1-DIMETHYLETHYL (1S,4S)-2,5-DIAZABICYCLO(2.2.1)HEPTANE-2-CARBOXYLATE n-(tert-butoxycarbonyl)-2,5-diazabicyclo[2.2.1]heptane (1S,4S)-2-Boc-2,5-diazabicyclo2.2.1üheptane, 97% (1S,4S)-2-N-T-BOC-2,5-DIAZABICYCLO[2.2.1]HEPTANE HYDROBROMIDE (1S,4S)-tert-butyl 2,5-diazabicyclo[2.2.1]heptane-2-carboxylate (1S,4S)-(-)-2-BOC-2,5-diazabicyclo[2.2.1]heptane,95% tert-Butyl (1S,4S)-2,5-diazabicyclo[2.2.1]heptan-2-carboxylate (1S,4S)-tert-butyl 2,5-diazabicyclo[2.2.1]heptane-2-carboxylate hydrochloride 2,5-Diazabicyclo[2.2.1]heptane-2-carboxylicacid, 1,1-diMethylethyl ester (1S,4S)-5-Boc-2,5-diazabicyclo[2.2.1]heptane (1S,4S)-2,5-DIAZA-BICYCLO(2.2.1)HEPTANE-2-CARBOXYLICACIDTERT-BUTYLESTER EOS-61878 (1S,4S)-(-)-2-Boc-2,5-diazabicyclo[2.2.1]heptane 95% 2,5-Diazabicyclo[2.2.1]heptane-2-carboxylicacid, 1,1-dimethylethyl ester, (1S,4S)- (1S,4S)-2-Boc-2,5-diazabicyclo(2.2.1)heptane methanesulfonic acid salt (1S,4S)-(?)-2-Boc-2,5-diazabicyclo[2.2.1]heptane (1S,4S)-N-Boc-2,5-diazabicyclo[2.2.1]heptane - [B6590] (1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptane 113451-59-5 C10H20Br2N2O2 Chiral Building Blocks Asymmetric Synthesis Heterocyclic Building Blocks Others Heterocycle-other series