반응식
C(O[C:4](=[NH:15])[CH2:5][S:6]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)(=[O:8])=[O:7])C.[O:16]1[C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=2[CH:18]=[C:17]1[C:25]([NH:27][NH2:28])=[O:26]>C(Cl)(Cl)Cl>[NH2:15][C:4](=[N:28][NH:27][C:25]([C:17]1[O:16][C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=2[CH:18]=1)=[O:26])[CH2:5][S:6]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)(=[O:8])=[O:7]참가 물질
4
실험 절차
3.4 g (0.0125 Mol) of 2-(phenylsulfonyl)-ethanimidic acid ethyl ester was stirred together with 2.2 g (0.015 mol) benzofuran-2-carboxylic acid hydrazide in 80 ml chloroform for 24 hours at 50° C. The resulting precipitate was filtered off and dried. 2.67 g of benzofuran-2-carboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide was obtained as off-white crystals. Mp.: 205-220° C.
후처리
- filtrationThe resulting precipitate was filtered off
- customdried
출처 및 근거
- ORD 기록
- ord-90d700d44f77465ebf7f7a966020652e
- 출처 데이터셋
- uspto-grants-2002_03
- 특허 번호
- US06355653B1
연결된 노트
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