Sodium Acetate → HCID 86616441, compound
Reaction equation
[CH2:1]([O:8][C:9](=[O:20])[C:10]1[CH:15]=[CH:14][C:13]([C:16](=O)[CH2:17]Br)=[N:12][CH:11]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:21][C:22]([NH2:24])=[S:23].CC([O-])=O.[Na+]>CCO>[CH2:1]([O:8][C:9](=[O:20])[C:10]1[CH:15]=[CH:14][C:13]([C:16]2[N:21]=[C:22]([NH2:24])[S:23][CH:17]=2)=[N:12][CH:11]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 6-(2-bromo-acetyl)-nicotinic acid benzyl ester (0.16 g, 0.48 mmol), thiourea (0.0.038 g), and NaOAc (0.051 g) in EtOH (6 mL) was stirred at room temperature overnight. The mixture was concentrated in vacuo to give the crude product 6-(2-Amino-thiazol-4-yl)-nicotinic acid benzyl ester.
Workup
- concentrationThe mixture was concentrated in vacuo
Sources & evidence
- ORD record
- ord-6bf6a643b04c4bd78ec1ebd23b6e84b6
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07595398B2
Reaction notes
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