Hydrochloric Acid → HCID 69053496, compound

HRID 456883Notes

Reaction equation

HRID 456883 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]1

Participants

5

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

  1. filtrationThe precipitated solids were collected by filtration
  2. washwashed with ether
  3. customdried

Sources & evidence

ORD record
ord-b25b6774dc8c4785beb5a3d775f2685e
Source dataset
uspto-grants-2007_03
Patent number
US07186742B2

Reaction notes

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