반응식
[CH3:1][S:2]([C:5]1[CH:6]=[C:7]([C:11]([CH3:21])=[CH:12][C:13]=1[O:14][C:15]1[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=1)[C:8](O)=[O:9])(=[O:4])=[O:3].[Cl-].C[N+]1C=CC=CC=1Cl.[Cl-].[NH2:32][C:33]([NH2:35])=[NH2+:34].C(N(C(C)C)C(C)C)C>CN1CCCC1=O>[NH2:34][C:33]([NH2:35])=[N:32][C:8](=[O:9])[C:7]1[C:11]([CH3:21])=[CH:12][C:13]([O:14][C:15]2[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=2)=[C:5]([S:2]([CH3:1])(=[O:4])=[O:3])[CH:6]=1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
1.0 g of 3-methylsulfonyl-4-(3-pyridyloxy)-6-methylbenzoic acid [obtainable by reacting 3-methylsulfonyl-4-chloro-6-methylbenzoic acid with 3-hydroxypyridine] is dissolved in 15 ml of 1-methylpyrrolidone, and 0.67 g of 1-methyl-2-chloropyridinium chloride is added to this solution, which is stirred for 15 min. 0.9 g of guanidinium chloride and 2.6 ml of N-ethyldiisopropylamine are then added, and the mixture is stirred at room temperature for one hour. Following customary working-up, N-diaminomethylene-3-methylsulfonyl-4-(3-pyridyloxy)-6-methylbenzamide is obtained, m.p. 221-224°.
후처리
- stirringthe mixture is stirred at room temperature for one hour
출처 및 근거
- ORD 기록
- ord-c2ebe1b38c8f4887a8c02cbc90e35665
- 출처 데이터셋
- uspto-grants-2000_02
- 특허 번호
- US06022883
연결된 노트
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