Hydrochloride methanol → HCID 67469208, compound

HRID 1850285Notes

Reaction equation

HRID 1850285 reaction equation
C(OC([N:8]1[CH2:11][CH:10]([C:12]2[C:17]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)=[CH:16][CH:15]=[CH:14][N:13]=2)[CH2:9]1)=O)(C)(C)C.[ClH:24].CO>>[ClH:24].[NH:8]1[CH2:9][CH:10]([C:12]2[C:17]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)=[CH:16][CH:15]=[CH:14][N:13]=2)[CH2:11]1

Participants

3

Reactant 2

HCID 21893726Hydrochloride methanolHCID 58547347HCID 58547347, compound

Product 1

HCID 67469208HCID 67469208, compoundYield 100%

Procedure

A mixture of 3-(3-phenyl-pyridin-2-yl)-azetidine-1-carboxylic acid tert-butyl ester (79) (130 mg, 0.60 mmol) in HCl/MeOH solution (5 mL) was stirred at RT for 30 min. Then the solvent was evaporated at 40° C. to give 2-Azetidin-3-yl-3-phenyl-pyridine hydrochloride (80) (100 mg, 100% yield) as a yellow solid.

Workup

  1. customThen the solvent was evaporated at 40° C.

Sources & evidence

ORD record
ord-13066d82b0b6445b95b28e1c3ad5932d
Source dataset
uspto-grants-2015_02
Patent number
US08957073B2

Reaction notes

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