Hydrochloride methanol → HCID 67469184, compound
Reaction equation
C(OC([N:8]1[CH2:11][CH:10]([C:12]2[CH:21]=[CH:20][C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[N:13]=2)[CH2:9]1)=O)(C)(C)C.[ClH:22].CO>>[ClH:22].[NH:8]1[CH2:9][CH:10]([C:12]2[CH:21]=[CH:20][C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[N:13]=2)[CH2:11]1Participants
3
Procedure
A solution of 3-quinolin-2-yl-azetidine-1-carboxylic acid tert-butyl ester (2.2 g, 7.75 mmol) in 4N HCl/MeOH (20 mL) was stirred at room temperature for 30 min. The reaction mixture was concentrated to give the crude product (1.70 g, 7.75 mmol, yield 100%).
Workup
- concentrationThe reaction mixture was concentrated
Sources & evidence
- ORD record
- ord-53a987eb0ac1402a81952d1c7079b83e
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08946230B2
Reaction notes
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