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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366234Generated: October 25, 2026

2-Aminothiazole → 6-(5-(phenylethynyl)thiophene-2-yl)-N-(2,4,4-trimethylpentane-2-yl)imidazo[2,1-b]thiazole-5-amine

https://huagongshe.com/reaction/1366234

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantSodium CarbonateHCID 10340—
ReactantPerchloric AcidHCID 24247—
Reactant1,1,3,3-Tetramethylbutyl isocyanideHCID 26725—
Reactant5-(Phenylethynyl)thiophene-2-carbaldehydeHCID 2737140—
SolventDichloromethaneHCID 6344—
Product6-(5-(phenylethynyl)thiophene-2-yl)-N-(2,4,4-trimethylpentane-2-yl)imidazo[2,1-b]thiazole-5-amineHCID 2487595837%

Reaction Steps

A solution of 400 mg (4.0 mmol) 2-aminothiazole, 1018 mg (4.8 mmol) 5-phenylethynyl-thiophene-2-carbaldehyde, 557 mg (4.0 mmol) (2,4,4-trimethylpentane-2-yl)-isocyanide and 400 μl of a 20% aq. perchloric acid was stirred in DCM (8 ml) for 5 d at RT. A 1 molar aq. Na2CO3 sol. was subsequently added. The phases were separated and the aqueous phase was extracted with DCM. The collected organic phases were washed with brine and dried over MgSO4. After filtering and removal of the solvent in a vacuum, a CC (AE/hexane 1:4) was performed with the residue, whereby 637 mg (1.47 mmol, 37%) 6-(5-(phenylethynyl)thiophene-2-yl)-N-(2,4,4-trimethylpentane-2-yl)imidazo[2,1-b]thiazole-5-amine was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893069B2
Source datasetuspto-grants-2011_02
ORD IDord-a2845a41776046949978bb693ed40b77
Source noteuspto-grants-2011_02