Oxalyl chloride → HCID 66680686, 화합물
반응식
C(Cl)(=O)C(Cl)=O.[Br:7][C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[N:13]([CH3:17])[C:12]([C:18]([OH:20])=O)=[CH:11]2.[NH2:21][C:22]1[CH:31]=[CH:30][C:29]([Cl:32])=[CH:28][C:23]=1[C:24]([O:26][CH3:27])=[O:25].O.C(=O)(O)[O-].[Na+]>CC(N(C)C)=O.C1COCC1.CN(C=O)C>[Br:7][C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[N:13]([CH3:17])[C:12]([C:18]([NH:21][C:22]1[CH:31]=[CH:30][C:29]([Cl:32])=[CH:28][C:23]=1[C:24]([O:26][CH3:27])=[O:25])=[O:20])=[CH:11]2참가 물질
실험 절차
A catalytic amount of DMF and 560 mg (4.41 mmol) of oxalyl chloride were added to a THF (8 mL) solution comprising 800 mg (3.15 mmol) of 5-bromo-1-methyl-1H-indole-2-carboxylic acid at 0° C., and the mixture was stirred at room temperature for 40 minutes. After the solvent was distilled off under reduced pressure, 8 mL of DMAc and 585 mg (3.15 mmol) of methyl 2-amino-5-chlorobenzoate were added to the residue in this order at 0° C., and the mixture was stirred at room temperature for 1 hour. After the completion of the reaction, saturated sodium bicarbonate water was added under ice-cooling, and the mixture was stirred. The resulting solids were collected by filtration, washed with water, and dried under reduced pressure at 50° C. for 3 hours, thereby giving 1.22 g of methyl 2-{[(5-bromo-1-methyl-1H-indol-2-yl)carbonyl]amino}-5-chlorobenzoate (yield: 92%).
후처리
- additionwere added to the residue in this order at 0° C.
- stirringthe mixture was stirred at room temperature for 1 hour
- additionwas added under ice-
- temperaturecooling
- stirringthe mixture was stirred
- filtrationThe resulting solids were collected by filtration
- washwashed with water
- customdried under reduced pressure at 50° C. for 3 hours
출처 및 근거
- ORD 기록
- ord-74ee75eb83284ee79d801fb6d7edb21d
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08785473B2
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