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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715944Generated: October 30, 2026

2-Aminothiazole → HCID 59465996, compound

https://huagongshe.com/reaction/1715944

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantHCID 59466191HCID 59466191—
SolventPyridineHCID 1049—
ProductHCID 59465996HCID 5946599632%

Reaction Steps

Prepared using general procedure 37. Under an N2 atmosphere, a mixture of the 4-(1-(2,2,2-trifluoroacetyl)pyrrolidin-2-yl)benzene-1-sulfonyl chloride (1.1 g, 5.8 mmol), 2-aminothiazole (0.58 g, 5.8 mmol), and pyridine (4.0 mL) was stirred at RT for 19 h. The crude product was purified via silica gel chromatography using 3% MeOH in CH2Cl2. The resulting oil was taken up in a 2:1 mixture of CH2Cl2:Et2O (12 mL) and cooled to 0° C. for 20 minutes. The formed precipitate was filtered off and dried under vacuum to obtain N-(thiazol-2-yl)-4-(1-(2,2,2-trifluoroacetyl)pyrrolidin-2-yl)benzene-sulfonamide as a white solid (750 mg, 32%). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=405.1; tR=2.68 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799822B2
Source datasetuspto-grants-2010_09
ORD IDord-0d588edd038a4783841d0e0572c1eab4
Source noteuspto-grants-2010_09