Ethanolamine → HCID 59312971, compound
Reaction equation
[NH2:1][C:2]1[N:3]=[C:4](S(C)(=O)=O)[S:5][C:6]=1[C:7]#[N:8].[NH2:13][CH2:14][CH2:15][OH:16]>CS(C)=O>[NH2:1][C:2]1[N:3]=[C:4]([NH:13][CH2:14][CH2:15][OH:16])[S:5][C:6]=1[C:7]#[N:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Example 89A is prepared in analogy to Example 48A from 4-amino-2-(methylsulphonyl)-1,3-thiazole-5-carbonitrile (Example 18A) (499 mg, 2.45 mmol) and 2-aminoethanol (300 mg, 4.91 mmol) in DMSO (80° C., 20 h). Removal of the solvent results in a crude product 527 mg (50% of theory) which is employed without further purification.
Workup
- customRemoval of the solvent
Sources & evidence
- ORD record
- ord-c30544b2ec40403dbfa88170336bd052
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08273752B2
Reaction notes
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