3-Pyridinamine, N,N-dimethyl- → Diphenylmethyl 7-[2-ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-(3-dimethylamino-1-pyridiniomethyl)-3-cephem-4-carboxylate-1-oxide chloride
反応式
[CH2:1]([O:3][N:4]=[C:5]([C:37]1[N:41]=[C:40]([NH2:42])[S:39][N:38]=1)[C:6]([NH:8][CH:9]1[C:35](=[O:36])[N:11]2[C:12]([C:19]([O:21][CH:22]([C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)=[O:20])=[C:13]([CH2:17][Cl:18])[CH2:14][S:15](=[O:16])[C@H:10]12)=[O:7])[CH3:2].[CH3:43][N:44]([CH3:51])[C:45]1[CH:46]=[N:47][CH:48]=[CH:49][CH:50]=1>O1CCCC1>[Cl-:18].[CH2:1]([O:3][N:4]=[C:5]([C:37]1[N:41]=[C:40]([NH2:42])[S:39][N:38]=1)[C:6]([NH:8][CH:9]1[C:35](=[O:36])[N:11]2[C:12]([C:19]([O:21][CH:22]([C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)=[O:20])=[C:13]([CH2:17][N+:47]3[CH:48]=[CH:49][CH:50]=[C:45]([N:44]([CH3:51])[CH3:43])[CH:46]=3)[CH2:14][S:15](=[O:16])[C@H:10]12)=[O:7])[CH3:2]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
A mixture of diphenylmethyl 7-[2-ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-chloromethyl-3-cephem-4-carboxylate-1-oxide (syn isomer) (3 g) and 3-dimethylaminopyridine (0.7 g) in tetrahydrofuran (20 ml) was stirred for 2.5 hours at 48° to 50° C. The resulting precipitate was filtered, washed with tetrahydrofuran and dried to give diphenylmethyl 7-[2-ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetamido]-3-(3-dimethylamino-1-pyridiniomethyl)-3-cephem-4-carboxylate-1-oxide chloride (syn isomer) (3.18 g), mp 120° to 130° C. (dec.).
後処理
- filtrationThe resulting precipitate was filtered
- washwashed with tetrahydrofuran
- customdried
出典と根拠
- ORDレコード
- ord-6f97d0a7d6d54560832c5963a9fd8dfa
- 出典データセット
- uspto-grants-1985_06
- 特許番号
- US04521413
反応ノート
読み込み中…