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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366237Generated: October 31, 2026

2-Aminothiazole → HCID 24876135, compound

https://huagongshe.com/reaction/1366237

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantSodium CarbonateHCID 10340—
ReactantTert-Butyl isocyanideHCID 23577—
ReactantPerchloric AcidHCID 24247—
ReactantHCID 87217901HCID 87217901—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 24876135HCID 2487613534.2%

Reaction Steps

A solution of 380 mg (3.8 mmol) 2-amino-thiazole, 749 mg (3.8 mmol) 5-(pyridine-2-yl-ethynyl)-furan-2-carbaldehyde, 378 mg (3.8 mmol) tert.butyl-isonitril and 73 μl of a 70% aq. perchloric acid in chloroform (2 ml) was heated to 45° C. while being stirred for 16 h. Dilution with DCM was subsequently performed and a 1 molar aq. Na2CO3 sol. was added. After 10 min of stirring at RT, the phases were separated. The aqueous phase was extracted with DCM. The collected organic phases were dried over Na2SO4, filtered and concentrated in a vacuum. 472 mg (1.3 mmol, 34%) N-tert-butyl-6-(5-(pyridine-2-ylethynyl)furan-2-yl)imidazo[2,1-b]thiazole-5-amine was obtained by CC (AE) with the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893069B2
Source datasetuspto-grants-2011_02
ORD IDord-44ffb026b87549be8c5962a9ad703445
Source noteuspto-grants-2011_02