Dichloromethane → HCID 23463661, compound

HRID 224235Notes

Reaction equation

HRID 224235 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

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

  1. stirringThe reaction mixture is stirred for 1 hour
  2. washThe organic layer is washed with water
  3. dry with materialdried over sodium sulfate
  4. customevaporated
  5. customto remove the solvent
  6. 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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