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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366236Generated: October 25, 2026

2-Aminothiazole → N-(2,4,4-trimethylpentane-2-yl)imidazo[2,1-b]thiazole-5-amine

https://huagongshe.com/reaction/1366236

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantSodium CarbonateHCID 10340—
ReactantPerchloric AcidHCID 24247—
Reactant1,1,3,3-Tetramethylbutyl isocyanideHCID 26725—
Reactant5-Pyridin-2-ylethynyl-thiophene-2-carbaldehydeHCID 86230190—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductN-(2,4,4-trimethylpentane-2-yl)imidazo[2,1-b]thiazole-5-amineHCID 131728708—

Reaction Steps

A solution of 5.0 g (50.0 mmol) 2-amino-thiazole, 10.7 g (50.0 mmol) 5-(pyridine-2-yl-ethynyl)-thiophene-2-carbaldehyde, 7.0 g (50.0 mmol) (2,4,4-trimethylpentane-2-yl)-isocyanide and 1.0 ml of a 70% aq. perchloric acid in chloroform (25 ml) was heated to 50° C. while being stirred for 5 d. 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. 11.86 g (27.3 mmol, 55%) 6-(5-pyridine-2-ylethynyl)thiophene-2-yl)-N-(2,4,4-trimethylpentane-2-yl)imidazo[2,1-b]thiazole-5-amine was obtained by multiple crystallisation of the residue from AE.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893069B2
Source datasetuspto-grants-2011_02
ORD IDord-d1e8e57cc9214cd59a55f5fd75d599fc
Source noteuspto-grants-2011_02