Triethylamine → HCID 15053573, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:10]2[S:11][CH:12]=[C:13]([CH2:15][OH:16])[N:14]=2)=[CH:5][CH:4]=1.C(N(CC)CC)C>CS(C)=O>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([NH:9][C:10]2[S:11][CH:12]=[C:13]([CH:15]=[O:16])[N:14]=2)=[CH:7][CH:8]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The reaction described in Preparation 44 was repeated, but using 3 g of 2-p-anisidinothiazol-4-yl-methanol, 6.1 g of pyridine sulfur trioxide complex, 5.3 ml of triethylamine and 90 ml of dimethyl sulfoxide, giving the title compound as pale brown crystals.
Workup
- customThe reaction described in Preparation 44
Sources & evidence
- ORD record
- ord-939d4a7f8449472989fe5383d809c8d6
- Source dataset
- uspto-grants-1990_06
- Patent number
- US04933355
Reaction notes
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