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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | 1,1,3,3-Tetramethylbutyl isocyanide | HCID 26725 | — |
| Reactant | 5-Pyridin-2-ylethynyl-thiophene-2-carbaldehyde | HCID 86230190 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2,4,4-trimethylpentane-2-yl)imidazo[2,1-b]thiazole-5-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893069B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-d1e8e57cc9214cd59a55f5fd75d599fc |
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| Source note | uspto-grants-2011_02 |
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