반응식
[NH2:1][C:2]1[N:7]=[C:6]([Cl:8])[CH:5]=[C:4]([O:9][CH3:10])[N:3]=1.[N:11]([S:14]([C:17]1[CH:27]=[CH:26][CH:25]=[CH:24][C:18]=1[C:19]([O:21][CH2:22][CH3:23])=[O:20])(=[O:16])=[O:15])=[C:12]=[O:13]>C(Cl)Cl>[CH2:22]([O:21][C:19](=[O:20])[C:18]1[CH:24]=[CH:25][CH:26]=[CH:27][C:17]=1[S:14]([NH:11][C:12]([NH:1][C:2]1[N:7]=[C:6]([Cl:8])[CH:5]=[C:4]([O:9][CH3:10])[N:3]=1)=[O:13])(=[O:15])=[O:16])[CH3:23]참가 물질
4
실험 절차
To 1.0 g of 2-amino-4-chloro-6-methoxypyrimidine suspended in 25 ml of dry CH2Cl2 was added 1.53 g of ethyl 2-(isocyanatosulfonyl)benzoate (prepared by procedures taught in U.S. Pat. No. 4,305,884). The reaction mixture was stirred at ambient temperature for three days. The solvent was stripped and the product was recrystallized from butyl chloride to give a white solid with m.p. 198°-201°.
후처리
- customprepared by procedures
- customthe product was recrystallized from butyl chloride
- customto give a white solid with m.p. 198°-201°
출처 및 근거
- ORD 기록
- ord-eb4dcd838c1f489f9e4d50c14c536e5d
- 출처 데이터셋
- uspto-grants-1987_02
- 특허 번호
- US04645530
연결된 노트
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