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147081-59-2

147081-59-2 Structure

147081-59-2 Structure
IdentificationBack Directory
[Name]

1-Pyrrolidinecarboxylicacid,3-(methylamino)-,1,1-dimethylethylester,(3S)-(9CI)
[CAS]

147081-59-2
[Synonyms]

-tert-Butyl 3-(methylamino)
1-N-Boc-(S)-(methylamino)-pyrrolidine
1-N-Boc-3-(S)-(Methylamino) pyrrolidine
ert-butyl(3S)-3-(methylamino)pyrrolidine-1-carboxylate
tert-butyl (S)-3-(methylamino)pyrrolidine-1-carboxylate
tert-Butyl-(3S)-3-(methylamino)pyrrolidine-1-carboxylate
(3S)-(Methylamino)pyrrolidine-1-carboxylic acid tert-butyl ester
(3S)-3-(Methylamino)-1-pyrrolidinecarboxylic acid tert-butyl ester
(3S)-3-(Methylamino)-1-Pyrrolidinecarboxylicacid 1,1-imethylethyl ester
1-Pyrrolidinecarboxylicacid,3-(MethylaMino)-,1,1-diMethylethylester,(3S)-
1-Pyrrolidinecarboxylicacid,3-(methylamino)-,1,1-dimethylethylester,(3S)-(9CI)
1-Pyrrolidinecarboxylicacid,3-(methylamino)-,1,1-dimethylethylester,(3S)-(9CI) USP/EP/BP
[Molecular Formula]

C10H20N2O2
[MDL Number]

MFCD09752962
[MOL File]

147081-59-2.mol
[Molecular Weight]

200.28
Chemical PropertiesBack Directory
[Boiling point ]

269℃
[density ]

1.03
[Fp ]

117℃
[storage temp. ]

Keep in dark place,Sealed in dry,2-8°C
[pka]

10.02±0.20(Predicted)
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P305+P351+P338
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

1-Pyrrolidinecarboxylicacid,3-(methylamino)-,1,1-dimethylethylester,(3S)-(9CI)(147081-59-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-Pyrrolidinecarboxylic acid, 3-(formylamino)-, 1,1-dimethylethyl ester, (3S)-

892390-43-1

1-Pyrrolidinecarboxylicacid,3-(methylamino)-,1,1-dimethylethylester,(3S)-(9CI)

147081-59-2

To a stirred solution of (3S)-3-(formylamino)pyrrolidine-1-carboxylic acid tert-butyl ester (2.29 g, 10 mmol) in tetrahydrofuran (35 ml) at 0°C was slowly added a tetrahydrofuran solution of 1 M borane (32 ml, 32 mmol). The reaction mixture was stirred at room temperature for 18 h. The reaction was quenched with methanol (10 ml) followed by vacuum concentration. The resulting white solid was redissolved in methanol (30 ml) and heated to reflux for 18 hours. Finally, the solvent was removed by vacuum evaporation to afford (S)-1-Boc-3-(methylamino)pyrrolidine as a light yellow oil (2.45 g, 12.2 mmol, 100% yield). The product was characterized by 1HNMR (400 MHz, CDCl3): δ 1.45 (s, 9H), 1.47-1.77 (m, 2H), 1.71 (m, 1H), 2.03 (m, 1H), 2.43 (s, 3H), 3.04-3.26 (m, 1H), 3.29-3.58 (m, 2H); LRMS m/z ELSD- apci+ 201 [mh]+.

[References]

[1] Patent: WO2006/64336, 2006, A2. Location in patent: Page/Page column 43-44
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