Hydrochloric Acid → HCID 69053496, compound
Reaction equation
[NH2:1][CH2:2][CH:3]([OH:30])[CH2:4][N:5]1[C:9]([CH3:10])=[CH:8][C:7]([C:11]2[CH:12]=[CH:13][C:14]([Cl:29])=[C:15]([CH:28]=2)[C:16]([NH:18][CH2:19][C:20]2([OH:27])[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]2)=[O:17])=[N:6]1.Cl>ClCCl.CCOCC>[ClH:29].[NH2:1][CH2:2][CH:3]([OH:30])[CH2:4][N:5]1[C:9]([CH3:10])=[CH:8][C:7]([C:11]2[CH:12]=[CH:13][C:14]([Cl:29])=[C:15]([CH:28]=2)[C:16]([NH:18][CH2:19][C:20]2([OH:27])[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]2)=[O:17])=[N:6]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 5-[1-(3-Amino-2-hydroxy-propyl)-5-methyl-1H-pyrazol-3-yl]-2-chloro-N-(1-hydroxy-cycloheptylmethyl)-benzamide (1.05 g, 2.41 mmol) in dichloromethane (10.0 mL) was added 2.0 N Hydrochloric acid in diethylether (4.0 mL, 8.0 mmol). The mixture was diluted with ether (50 mL) and stirred for 15 min. The precipitated solids were collected by filtration, washed with ether and dried to give title compound (1.0 g): LCMS (m/z) 435.3 M+1.
Workup
- filtrationThe precipitated solids were collected by filtration
- washwashed with ether
- customdried
Sources & evidence
- ORD record
- ord-7ed41f1bd8864b6698a6b0be4ad8c7d5
- Source dataset
- uspto-grants-2009_06
- Patent number
- US07553972B2
Reaction notes
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