Chlorosuccinimide → HCID 21469013, compound

HRID 1938332Notes

Reaction equation

HRID 1938332 reaction equation
[S:1]1[C:10]2[C:9]3[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=3[N:7]([C:15]([C:17]3[CH:22]=[CH:21][C:20]([NH:23][C:24](=[O:33])[C:25]4[CH:30]=[CH:29][CH:28]=[C:27]([F:31])[C:26]=4[CH3:32])=[CH:19][CH:18]=3)=[O:16])[CH2:6][CH2:5][C:4]=2[CH:3]=[CH:2]1.[Cl:34]N1C(=O)CCC1=O>C(OCC)(=O)C>[Cl:34][C:2]1[S:1][C:10]2[C:9]3[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=3[N:7]([C:15]([C:17]3[CH:22]=[CH:21][C:20]([NH:23][C:24](=[O:33])[C:25]4[CH:30]=[CH:29][CH:28]=[C:27]([F:31])[C:26]=4[CH3:32])=[CH:19][CH:18]=3)=[O:16])[CH2:6][CH2:5][C:4]=2[CH:3]=1

Participants

4

Procedure

To a solution of 0.457 g (1.0 mmol) of N-[4-[(4,5-dihydro-6H-thieno[3,2-d][1]benzazepin-6-yl)carbonyl]phenyl]-2-methyl-3-fluorobenzamide in 25 ml of ethyl acetate is added 1.0 mmol of N-chlorosuccinimide. The mixture is stirred overnight and filtered. The filtrate is washed with water, 1N HCl, 1M NaHCO3, H2O and dried (Na2SO4). The solvent is removed to give the product as a solid.

Workup

  1. filtrationfiltered
  2. washThe filtrate is washed with water, 1N HCl, 1M NaHCO3, H2O
  3. dry with materialdried (Na2SO4)
  4. customThe solvent is removed

Sources & evidence

ORD record
ord-2e70ee095b3f42da8a726f9060fd6f1b
Source dataset
uspto-grants-1997_12
Patent number
US05693635

Reaction notes

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