反応式
[OH:1][CH:2]1[CH2:7][NH:6][CH2:5][C:4]2[S:8][CH:9]=[CH:10][C:3]1=2.[C:11]1([N:17]=[C:18]=[S:19])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>C1C=CC=CC=1.C(O)C>[OH:1][CH:2]1[CH2:7][N:6]([C:18](=[S:19])[NH:17][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH2:5][C:4]2[S:8][CH:9]=[CH:10][C:3]1=2参加物
5
実験手順
To a solution of 4-hydroxy-4,5,6,7-tetrahydro-thieno[2,3-c]-pyridine (5.8 g; 37.4 mmoles) in benzene (60 cc) and 95% ethanol (30 cc) is added dropwise a mixture of phenyl isothiocyanate (5.05 g; 37.4 mmoles) in benzene (20 cc). After stirring during 2.5 hours at room temperature, the resulting precipitate is filtered off, washed with ether and dried in vacuo (M.p. = 168° C; yield: 79%).
後処理
- filtrationthe resulting precipitate is filtered off
- washwashed with ether
- customdried in vacuo (M.p. = 168° C; yield: 79%)
出典と根拠
- ORDレコード
- ord-3d69328eaf824cdc8b008681d392276f
- 出典データセット
- uspto-grants-1978_02
- 特許番号
- US04076819
関連ノート
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