Sodium Hydroxide → Methyl 5-ethyl-1,3-thiazole-4-carboxylate
Reaction equation
N([O-])=O.[Na+].N[C:6]1[S:7][C:8]([CH2:15][CH3:16])=[C:9]([C:11]([O:13][CH3:14])=[O:12])[N:10]=1.[OH-].[Na+]>O.O[PH2]=O.C([O-])(O)=O.[Na+]>[CH2:15]([C:8]1[S:7][CH:6]=[N:10][C:9]=1[C:11]([O:13][CH3:14])=[O:12])[CH3:16]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 3
Conditions
- Temperature
- 0 °C
Procedure
The following diazotization step was adapted from Barton, A.; Breukelman, S. P.; Kaye, P. T.; Meakins, G. D.; Morgan, D. J. J. C. S. Perkin Trans I 1982, 159-164: A solution of NaNO2 (150 mg, 2.17 mmol) in water (1.0 mL) was added dropwise to a stirred, cold (0° C.) solution of methyl 2-amino-5-ethyl-1,3-thiazole-4-carboxylate (186 mg, 1.0 mmol) in 50% H3PO2 (3.2 mL). The mixture was stirred at 0° C. for 1 h and allowed to warm up to room temperature where it stirred further for 2 h. After recooling to 0° C., the mixture was treated slowly with a solution of NaOH (85 mg) in water (10 mL). The mixture was then diluted with saturated NaHCO3 solution and extracted twice with ether. The organic layers were combined, dried over MgSO4 and concentrated to give methyl 5-ethylthiazole-4-carboxylate (i.e. Cap-173, step a) (134 mg, 78%) as an orange oil (85% pure) which was used directly in the next reaction. Rt=1.58 min (Cond.-MD1); LC/MS: Anal. Calcd. for [M+H]+ C7H10NO2S: 172.05; found: 172.05.
Workup
- temperatureto warm up to room temperature where it
- stirringstirred further for 2 h
- customAfter recooling to 0° C.
- extractionextracted twice with ether
- dry with materialdried over MgSO4
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-9ffad48a6de74f2fa1bf740e137f4fea
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08809548B2
Reaction notes
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