反応式
[Cl:1][C:2]1[C:3]([S:8]([NH2:11])(=[O:10])=[O:9])=[N:4][CH:5]=[CH:6][CH:7]=1.[C:12](=O)([O:14]C1C=CC=CC=1)N.[CH3:22][O:23][C:24]1[CH:29]=[C:28]([O:30][CH3:31])[N:27]=[C:26]([NH2:32])[N:25]=1.C1CCN2C(=NCCC2)CC1.Cl.[OH2:45]>C(#N)C>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[N+:4]([O-:45])[C:3]=1[S:8]([NH:11][C:12]([NH:32][C:26]1[N:27]=[C:28]([O:30][CH3:31])[CH:29]=[C:24]([O:23][CH3:22])[N:25]=1)=[O:14])(=[O:9])=[O:10]参加物
8
反応物 6
生成物 1
試薬・触媒・溶媒 1
実験手順
To a stirring solution of the N-oxide of 3-chloro-2-pyridinesulfonamide (85 mg, 0.4 mmol) and the phenyl carbamate of 4,6-dimethoxy-2-aminopyrimidine (114 mg, 0.40 mmol) in acetonitrile was added DBU (62 mg, 0.40 mmol). Addition of H2O followed by 5% HCl caused a precipitate to form which was collected, m.p. 144°-147° C. NMR (200 MHz, d6 -DMSO) δ 3.91 (s, 6H), 5.998 (s, 1H), 7.7 (m, 2H), 8.4 (d, 1H), 10.8 (br s, 1H) and 13.1 (br s, 1H); IR (nujol) 1710 (s) cm-1 ; mass spectrum m/e 390 (M+, calc. for C12H12ClN5O6S 389+1).
後処理
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出典と根拠
- ORDレコード
- ord-99f0a07897394466824deb4e90cc583d
- 出典データセット
- uspto-grants-1988_12
- 特許番号
- US04789465
関連ノート
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