Triethylamine → HCID 15053581, compound
Reaction equation
[N:1]1([C:7]2[S:8][CH:9]=[C:10]([CH2:12][OH:13])[N:11]=2)[CH2:6][CH2:5][S:4][CH2:3][CH2:2]1.C(N(CC)CC)C>CS(C)=O>[N:1]1([C:7]2[S:8][CH:9]=[C:10]([CH:12]=[O:13])[N:11]=2)[CH2:6][CH2:5][S:4][CH2:3][CH2:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The reaction described in Preparation 44 was repeated, but using 1.2 g of 2-(thiomorpholin-4-yl)thiazol-4-ylmethanol, 2.65 g of sulfur trioxide pyridine complex, 1.68 g of triethylamine and 30 ml of dimethyl sulfoxide, giving the title compound as a colorless powder.
Workup
- customThe reaction described in Preparation 44
Sources & evidence
- ORD record
- ord-eed5622d70a34a3bb1da49ceb16e0565
- Source dataset
- uspto-grants-1990_06
- Patent number
- US04933355
Reaction notes
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