반응식
O=C1C2C(=CC=CC=2)C(=O)[N:3]1[CH2:12]/[CH:13]=[CH:14]/[C:15]1[CH:20]=[CH:19][C:18]([NH:21][C:22]([C:24]2[C:25]([C:30]3[CH:35]=[CH:34][C:33]([C:36]([F:39])([F:38])[F:37])=[CH:32][CH:31]=3)=[CH:26][CH:27]=[CH:28][CH:29]=2)=[O:23])=[CH:17][CH:16]=1.NN>C(O)C>[NH2:3][CH2:12]/[CH:13]=[CH:14]/[C:15]1[CH:20]=[CH:19][C:18]([NH:21][C:22]([C:24]2[C:25]([C:30]3[CH:31]=[CH:32][C:33]([C:36]([F:37])([F:38])[F:39])=[CH:34][CH:35]=3)=[CH:26][CH:27]=[CH:28][CH:29]=2)=[O:23])=[CH:17][CH:16]=1참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
A mixture of intermediate (2) (0.005 mol) and an aqueous hydrazine solution (0.005 mol) in ethanol (30 ml) was stirred and refluxed for 2 hours. The precipitate was filtered and washed with ethanol. Water was added. The suspension was basified with NaOH and filtered over celite. Celite was washed with ethyl acetate. The filtrate was extracted with ethyl acetate and washed with K2CO3, then with NaCl. The organic layer was separated, dried, filtered, and the solvent was evaporated. The residue was crystallized from ACN. The precipitate was filtered off and dried, yielding 2.5 g of N-[4-[(1E)-3-amino-1-propenyl]phenyl]-4′-(trifluoromethyl)-[1,1′-biphenyl]-2-carboxamide (intermediate 3; mp. 190° C.).
후처리
- temperaturerefluxed for 2 hours
- filtrationThe precipitate was filtered
- washwashed with ethanol
- additionWater was added
- filtrationfiltered over celite
- washCelite was washed with ethyl acetate
- extractionThe filtrate was extracted with ethyl acetate
- washwashed with K2CO3
- customThe organic layer was separated
- customdried
- filtrationfiltered
- customthe solvent was evaporated
- customThe residue was crystallized from ACN
- filtrationThe precipitate was filtered off
- customdried
출처 및 근거
- ORD 기록
- ord-6e274d00fdbe43af8fdd80d9bd1fa93e
- 출처 데이터셋
- uspto-grants-2009_05
- 특허 번호
- US07538124B2
연결된 노트
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