Hydrochloric Acid → (R)-N-(5-(2-(3-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-yl)-6-methoxypicolinamide hydrochloride
Reaction equation
CO.[F:3][C:4]1[CH:5]=[C:6]([C@H:10]2[CH2:14][CH2:13][CH2:12][N:11]2[C:15]2[CH:20]=[CH:19][N:18]3[N:21]=[CH:22][C:23]([NH:24][C:25](=[O:34])[C:26]4[CH:31]=[CH:30][CH:29]=[C:28]([O:32][CH3:33])[N:27]=4)=[C:17]3[N:16]=2)[CH:7]=[CH:8][CH:9]=1.[ClH:35]>O1CCOCC1>[ClH:35].[F:3][C:4]1[CH:5]=[C:6]([C@H:10]2[CH2:14][CH2:13][CH2:12][N:11]2[C:15]2[CH:20]=[CH:19][N:18]3[N:21]=[CH:22][C:23]([NH:24][C:25](=[O:34])[C:26]4[CH:31]=[CH:30][CH:29]=[C:28]([O:32][CH3:33])[N:27]=4)=[C:17]3[N:16]=2)[CH:7]=[CH:8][CH:9]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a methanol (1 mL) solution of (R)—N-(5-(2-(3-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-yl)-6-methoxypicolinamide (10.1 mg, 0.0234 mmol) was added HCl as a solution is dioxane (30 μL). After 30 minutes, the reaction was concentrated to provide (R)—N-(5-(2-(3-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-yl)-6-methoxypicolinamide hydrochloride as a yellow solid.
Workup
- concentrationthe reaction was concentrated
Sources & evidence
- ORD record
- ord-e0dba49ac0fb4dfba9e946b11a144019
- Source dataset
- uspto-grants-2014_10
- Patent number
- US08865698B2
Reaction notes
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