Dichloromethane → HCID 86652152, compound

HRID 1626035Notes

Reaction equation

HRID 1626035 reaction equation
Cl[C:2]([O:4][CH:5]([Cl:7])[CH3:6])=[O:3].ClCCl.[CH3:11][NH:12][CH2:13][C:14]([O:16][CH:17]1[CH2:23][CH2:22][CH2:21][N:20]([C:24](=[O:42])[C:25]2[CH:30]=[CH:29][C:28]([NH:31][C:32](=[O:40])[C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][C:34]=3[CH3:39])=[CH:27][C:26]=2[CH3:41])[C:19]2[CH:43]=[CH:44][C:45]([Cl:47])=[CH:46][C:18]1=2)=[O:15].CN1CCOCC1>C(OCC)(=O)C>[Cl:7][CH:5]([O:4][C:2]([CH2:11][NH:12][CH2:13][C:14]([O:16][CH:17]1[CH2:23][CH2:22][CH2:21][N:20]([C:24](=[O:42])[C:25]2[CH:30]=[CH:29][C:28]([NH:31][C:32](=[O:40])[C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][C:34]=3[CH3:39])=[CH:27][C:26]=2[CH3:41])[C:19]2[CH:43]=[CH:44][C:45]([Cl:47])=[CH:46][C:18]1=2)=[O:15])=[O:3])[CH3:6]

Participants

6

Procedure

1-Chloroethyl chloroformate (0.12 ml, 1.2 mmol) was added dropwise to a dichloromethane (10 ml) solution of 7-chloro-1-[2-methyl-4-(2-methylbenzamido)benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl methylaminoacetate (0.60 g, 1.2 mmol), and the mixture was cooled with ice. Then N-methylmorpholine (0.15 ml, 1.4 mmol) was gradually added dropwise thereto. After the resultant mixture was stirred at room temperature for 1 hour, the reaction mixture was diluted with ethyl acetate, washed with water and an aqueous saturated sodium chloride solution, dried over sodium sulfate. After filtration and concentration, the residue was purified by silica gel chromatography (n-hexane:ethyl acetate) to obtain 0.67 g (93%) of 7-chloro-1-[2-methyl-4-(2-methylbenzamido)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl [(1-chloroethoxycarbonyl)methylamino]acetate as amorphous.

Workup

  1. temperaturethe mixture was cooled with ice
  2. washwashed with water
  3. dry with materialan aqueous saturated sodium chloride solution, dried over sodium sulfate
  4. filtrationAfter filtration and concentration
  5. customthe residue was purified by silica gel chromatography (n-hexane:ethyl acetate)

Sources & evidence

ORD record
ord-e18c90c9cb2d4d17982e704eb4766675
Source dataset
uspto-grants-2014_07
Patent number
US08785386B2

Reaction notes

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