ChemicalBook--->CAS DataBase List--->123696-02-6

123696-02-6

123696-02-6 Structure

123696-02-6 Structure
IdentificationBack Directory
[Name]

3-CHLORO-5-METHOXYPYRIDAZINE
[CAS]

123696-02-6
[Synonyms]

3-CHLORO-5-METHOXYPYRIDAZINE
Pyridazine, 3-chloro-5-methoxy-
3-Chloro-5-Methoxypyridazine HCl
3-Chloro-5-methoxypyridazine, HCl salt
3-CHLORO-5-METHOXYPYRIDAZINE ISO 9001:2015 REACH
[EINECS(EC#)]

200-001-2
[Molecular Formula]

C5H5ClN2O
[MDL Number]

MFCD08236839
[MOL File]

123696-02-6.mol
[Molecular Weight]

144.56
Chemical PropertiesBack Directory
[Boiling point ]

285 ºC
[density ]

1.292
[Fp ]

126 ºC
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

2.45±0.10(Predicted)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C5H5ClN2O/c1-9-4-2-5(6)8-7-3-4/h2-3H,1H3
[InChIKey]

XLGRINRFBNCHQS-UHFFFAOYSA-N
[SMILES]

C1(Cl)=NN=CC(OC)=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

3-Chloro-5-methoxypyridazine is used to synthesize potent and selective inhibitors of glycogen synthase kinase 3 with good cellular efficacy.
[Synthesis]

5-METHOXYPYRIDAZIN-3(2H)-ONE

123696-01-5

3-CHLORO-5-METHOXYPYRIDAZINE

123696-02-6

5-Methoxypyridazin-3(2H)-one (250 mg, 1.98 mmol) was used as starting material and suspended in phosphoryl chloride (1.5 mL, 16 mmol). The reaction mixture was stirred at 100 °C for 10 min. After completion of the reaction, the mixture was slowly poured into ice water and the pH was adjusted to alkaline by adding sodium carbonate. Subsequently, the mixture was extracted with ether and the organic phases were combined and dried with anhydrous magnesium sulfate. After filtration, the solvent was removed by distillation under reduced pressure. The resulting residue was recrystallized with 1,2-dichloroethane to give 130 mg of 3-chloro-5-methoxypyridazine in 45% yield. The product was analyzed by LC-MS (Method 5): r = 0.85 mm; MS (ESIpos): m/z = 145 [M + H]+. 1H-NMR (400 MHz, DMSO-d6) δ (ppm): 2.495 (0.78), 2.499 (1.07), 2.503 (0.84), 3.317 (11.94). 3.944 (16.00), 7.528 (2.28), 7.534 (2.29), 8.988 (2.34), 8.994 (2.34).

[References]

[1] Journal of Heterocyclic Chemistry, 1995, vol. 32, # 5, p. 1473 - 1476
[2] Journal of Medicinal Chemistry, 2004, vol. 47, # 19, p. 4716 - 4730
[3] Monatshefte fuer Chemie, 1989, vol. 120, p. 329 - 342
[4] Patent: WO2017/102091, 2017, A1. Location in patent: Page/Page column 455; 456
Spectrum DetailBack Directory
[Spectrum Detail]

3-CHLORO-5-METHOXYPYRIDAZINE(123696-02-6)1HNMR
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