Triethylamine → HCID 20437026, compound
Reaction equation
[OH:1][C:2]1[CH:18]=[CH:17][C:5]([C:6]([C:8]2[S:12][C:11]([S:13]([NH2:16])(=[O:15])=[O:14])=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1.C(N(CC)CC)C.Cl[C:27]([O:29][CH2:30][CH:31]([CH3:33])[CH3:32])=[O:28]>CC(C)=O>[C:27](=[O:28])([O:1][C:2]1[CH:18]=[CH:17][C:5]([C:6]([C:8]2[S:12][C:11]([S:13](=[O:15])(=[O:14])[NH2:16])=[CH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1)[O:29][CH2:30][CH:31]([CH3:33])[CH3:32]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 5-(4-hydroxybenzoyl)thiophene-2-sulfonamide (0.00783 mole) in acetone (50 ml) at 0° C. is treated with triethylamine (0.00861 mole) followed by isobutyl chloroformate (0.00861 mole) dropwise, during 30 minutes at 0°-2° C.
Workup
- customduring 30 minutes
- customat 0°-2° C.
Sources & evidence
- ORD record
- ord-78af13bfa7244f1daef95b5aef4bfafa
- Source dataset
- uspto-grants-1984_12
- Patent number
- US04486444
Reaction notes
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