Dichloromethane → HCID 23463661, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=[O:35])[C:9]1[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:10]=1[N:16]1[C:20]([CH2:21][NH:22][C:23]([O:25][CH2:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)=[O:24])=[N:19][N:18]=[C:17]1[CH2:33][SH:34].C(N(CC)CC)C.C(Cl)Cl.[C:46](Cl)(=[O:50])[O:47][CH2:48][CH3:49]>O1CCCC1.O>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=[O:35])[C:9]1[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:10]=1[N:16]1[C:20]([CH2:21][NH:22][C:23]([O:25][CH2:26][C:27]2[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=2)=[O:24])=[N:19][N:18]=[C:17]1[CH2:33][S:34][C:46]([O:47][CH2:48][CH3:49])=[O:50]Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 2',5-dichloro-2-(5-carbobenzoxyaminomethyl-3-mercaptomethyl-1,2,4-triazol-4-yl)benzophenone (0.5 g), triethylamine (0.5 ml) and methylene chloride (10 ml) is added a solution of ethyl chlorocarbonate (0.5 ml) in tetrahydrofuran (8 ml) at 15° C. with stirring. The reaction mixture is stirred for 1 hour and poured into water. The organic layer is washed with water, dried over sodium sulfate and evaporated to remove the solvent. The residual oily material is chromatographed on a column of silica gel, whereby 2',5-dichloro-2-(5-carbobenzoxyaminomethyl-3-ethoxycarbonylthiomethyl-1,2,4-triazol-4-yl)benzophenone (0.5 g) is obtained as a colorless oil.
Workup
- stirringThe reaction mixture is stirred for 1 hour
- washThe organic layer is washed with water
- dry with materialdried over sodium sulfate
- customevaporated
- customto remove the solvent
- customThe residual oily material is chromatographed on a column of silica gel
Sources & evidence
- ORD record
- ord-c20fb361fe8d438a93676cc10c6947c6
- Source dataset
- uspto-grants-1980_11
- Patent number
- US04231930
Reaction notes
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