Nitronium tetrafluoroborate → 5-Acetyl-2-chloro-5,11-dihydro-11-ethyl-4-methyl-3-nitro-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one
반응식
[C:1]([N:4]1[C:10](=[O:11])[C:9]2[CH:12]=[CH:13][CH:14]=[N:15][C:8]=2[N:7]([CH2:16][CH3:17])[C:6]2[N:18]=[C:19]([Cl:23])[CH:20]=[C:21]([CH3:22])[C:5]1=2)(=[O:3])[CH3:2].F[B-](F)(F)F.[O:29]=[N+:30]=[O:31]>C(#N)C>[C:1]([N:4]1[C:10](=[O:11])[C:9]2[CH:12]=[CH:13][CH:14]=[N:15][C:8]=2[N:7]([CH2:16][CH3:17])[C:6]2[N:18]=[C:19]([Cl:23])[C:20]([N+:30]([O-:31])=[O:29])=[C:21]([CH3:22])[C:5]1=2)(=[O:3])[CH3:2]참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of 5-acetyl-2-chloro-5,11-dihydro-11-ethyl-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one (3.36 g) in acetonitrile (20 mL) cooled on ice was added nitronium tetrafluoroborate (85%, 2.26 g). The mixture was removed from the ice bath and was stirred for 5 hours. The reaction then was quenched with 10% potassium carbonate. Ethyl acetate was added and the organic phase was separated, washed, dried, and evaporated. Chromatography over silica gel gave 0.71 g of the title compound, which crystallized from diisopropyl ether, m.p. 140-141.
후처리
- customThe mixture was removed from the ice bath
- customThe reaction
- customthen was quenched with 10% potassium carbonate
- additionEthyl acetate was added
- customthe organic phase was separated
- washwashed
- customdried
- customevaporated
출처 및 근거
- ORD 기록
- ord-12e9883a74144360b23be1e7a0dbdb0e
- 출처 데이터셋
- uspto-grants-1997_04
- 특허 번호
- US05620974
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