Dimethylformamide → HCID 178437927, compound
Reaction equation
CN(C)C=O.Cl.[CH2:7]([C:9]1[S:13][C:12](=[NH:14])[N:11]([CH2:15][C:16]2[CH:21]=[CH:20][C:19]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=3[C:28]3[NH:32][N:31]=[N:30][N:29]=3)=[CH:18][CH:17]=2)[N:10]=1)[CH3:8].[C:33]12[C:41](=[O:42])[O:40][C:38](=[O:39])[C:34]=1[CH2:35][CH2:36][CH2:37]2>O>[CH2:7]([C:9]1[S:13][C:12](=[N:14][C:41]([C:33]2[CH2:37][CH2:36][CH2:35][C:34]=2[C:38]([OH:40])=[O:39])=[O:42])[N:11]([CH2:15][C:16]2[CH:17]=[CH:18][C:19]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=3[C:28]3[NH:29][N:30]=[N:31][N:32]=3)=[CH:20][CH:21]=2)[N:10]=1)[CH3:8]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To 2 ml of N,N-dimethylformamide, 200 mg of 5-ethyl-2-imino-3-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl-1,3,4-thiadiazoline hydrochloride and 76 mg of 1-cyclopentene-1,2-dicarboxylic anhydride were added and the resulting mixture was stirred at room temperature for 2 hours. Water was added to the reaction mixture and the crystals so precipitated were collected by filtration. The crystals were washed with water and ethanol and then dried, whereby 170 mg of the title compound was obtained.
Workup
- customthe crystals so precipitated
- filtrationwere collected by filtration
- washThe crystals were washed with water and ethanol
- customdried
Sources & evidence
- ORD record
- ord-bc686ad5b3314892ba70df5eda802127
- Source dataset
- uspto-grants-1999_06
- Patent number
- US05912353
Reaction notes
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