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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242448Generated: November 2, 2026

Phosphorus oxychloride → N-(2-Acetyl-5-methoxyphenyl)-2-((1-methylethyl)amino)-4-thiazolecarboxamide

https://huagongshe.com/reaction/2242448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(2-Amino-4-methoxyphenyl)ethan-1-oneHCID 10678615—
Reactant2-(Isopropylamino)thiazole-4-carboxylic acid hydrobromideHCID 11953489—
SolventPyridineHCID 1049—
ProductN-(2-Acetyl-5-methoxyphenyl)-2-((1-methylethyl)amino)-4-thiazolecarboxamideHCID 11953491101.8%

Reaction Conditions

Temperature-30 °C

Reaction Steps

A mixture of compound 69 (4.4 g, 16.5 mmol) and the aniline derivative 66 (2.75 g, 16.5 mmol) in pyridine (140 mL) was cooled to −30° C. (upon cooling, the clear solution became partially a suspension). POCl3 (3.3 mL, 35 mmol) was added slowly over a 5 min period. The mixture was stirred at −30° C. for 1 h, and was then allowed to assume rt. After stirring at rt for 1.5 h the reaction mixture was poured over ice, and the pH was adjusted to about 9-10 using solid and saturated NaHCO3. The crude product was extracted into CH2Cl2 (3×) and the combined organic phases were dried (MgSO4) and evaporated. The crude dark-beige solid was purified by flash column chromatography (hexane/EtOAc 55:45) to give compound 70 (5.6 g, 76%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671032B2
Source datasetuspto-grants-2010_03
ORD IDord-b0877d65bb664233b6271bdec90e99b9
Source noteuspto-grants-2010_03