Dichloromethane → HCID 86652152, compound
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
Reactant 4
Product 1
Reagents, catalysts & solvents 1
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
- temperaturethe mixture was cooled with ice
- washwashed with water
- dry with materialan aqueous saturated sodium chloride solution, dried over sodium sulfate
- filtrationAfter filtration and concentration
- 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
Loading…