반응식
[F:1][C:2]1[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][C:3]=1[C:4]([OH:6])=O.[O:14]1[C:18]2[CH:19]=[CH:20][C:21]([CH2:23][NH2:24])=[CH:22][C:17]=2[O:16][CH2:15]1.Cl.CN(C)CCCN=C=NCC.ON1C2C=CC=CC=2N=N1>CN(C)C=O>[F:1][C:2]1[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][C:3]=1[C:4]([NH:24][CH2:23][C:21]1[CH:20]=[CH:19][C:18]2[O:14][CH2:15][O:16][C:17]=2[CH:22]=1)=[O:6]참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
A mixture of 2-fluoro-5-nitrobenzoic acid (1.00 g), (1,3-benzodioxol-5-ylmethyl)amine (980 mg), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (1.55 g) and 1-hydroxybenzotriazole (1.09 g) in anhydrous dimethylformamide (10 mL) was stirred for 40 hours at ambient temperature. The mixture was partitioned between water and ethyl acetate. The separated organic layer was washed with an aqueous saturated sodium bicarbonate solution, 1N-hydrochloric acid, water and brine. Then, the resultant was dried over magnesium sulfate and evaporated in vacuo. The residue was triturated with diisopropyl ether to give 2-fluoro-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide as yellow powders (1.48 g).
후처리
- customThe mixture was partitioned between water and ethyl acetate
- washThe separated organic layer was washed with an aqueous saturated sodium bicarbonate solution, 1N-hydrochloric acid, water and brine
- dry with materialThen, the resultant was dried over magnesium sulfate
- customevaporated in vacuo
- customThe residue was triturated with diisopropyl ether
출처 및 근거
- ORD 기록
- ord-829a96a6ccff41a995f08c54de850f1f
- 출처 데이터셋
- uspto-grants-2002_05
- 특허 번호
- US06384080B1
연결된 노트
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