Hydrochloric Acid → N-((1S,2R)-1-(3,5-difluorobenzyl)-3-{[6-ethyl-3,4-dihydro-2H-chromen-4-yl]amino}-2-hydroxypropyl)acetamide

HRID 1296085Notes

Reaction equation

HRID 1296085 reaction equation
CC(OC)(C)C.C(Cl)Cl.[F:10][C:11]1[CH:12]=[C:13]([CH:36]=[C:37]([F:39])[CH:38]=1)[CH2:14][C@H:15]([NH:32][C:33](=[O:35])[CH3:34])[C@H:16]([OH:31])[CH2:17][NH:18][C@@H:19]1[C:28]2[C:23](=[CH:24][CH:25]=[C:26]([CH2:29][CH3:30])[CH:27]=2)[O:22][CH2:21][CH2:20]1.Cl>CCOCC.CO>[F:10][C:11]1[CH:12]=[C:13]([CH:36]=[C:37]([F:39])[CH:38]=1)[CH2:14][C@H:15]([NH:32][C:33](=[O:35])[CH3:34])[C@H:16]([OH:31])[CH2:17][NH:18][CH:19]1[C:28]2[C:23](=[CH:24][CH:25]=[C:26]([CH2:29][CH3:30])[CH:27]=2)[O:22][CH2:21][CH2:20]1

Participants

7

Procedure

To a MTBE (20 ml), CH2Cl2 (5 ml), MeOH (0.5 ml) solution of N-((1S,2R)-1-(3,5-difluorobenzyl)-3-{[(4S)-6-ethyl-3,4-dihydro-2H-chromen-4-yl]amino}-2-hydroxypropyl)acetamide (0.2 g, 0.5 mmol) was added 1N HCl in Et2O (0.38 ml) and the mixture stirred at room temperature. The final white solid was isolated by removing the solvent and tritration with Et2O. HRMS (ESI+) calcd for C23H28F2N2O3 m/z 419.2146 (M+H)+. Found 419.2166.

Workup

  1. customThe final white solid was isolated
  2. customby removing the solvent and tritration with Et2O

Sources & evidence

ORD record
ord-7923b44806fa41e1a63879a07c520ffb
Source dataset
uspto-grants-2007_07
Patent number
US07244725B2

Reaction notes

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