HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923645Generated: October 30, 2026
Isopropylamine → 2-Chloro-thiazole-5-carboxylic acid isopropylamide
https://huagongshe.com/reaction/1923645
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | Ethyl 2-chloro-1,3-thiazole-5-carboxylate | HCID 19017727 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Chloro-thiazole-5-carboxylic acid isopropylamide | HCID 66643738 | 94% |
Reaction Steps
To a stirred solution of isopropylamine (123 mg, 2.08 mmol) in dioxane (5 mL) under argon and at room temperature was added trimethylaluminium (1.04 mL of a 2M solution in toluene, 2.08 mmol). After 1 h, a solution of 2-chloro-thiazole-5-carboxylic acid ethyl ester (100 mg, 0.522 mmol) in dioxane (5 mL) was added and the reaction mixture warmed to 90° C. After 6 h, the reaction mixture was cooled, quenched with Seignettes's salt solution and water, then extracted with dichloromethane. The combined organic extracts were dried, filtered and concentrated. Purification by chromatography (silica, 0 to 30% ethyl acetate in heptane) gave the title compound (100 mg, 94%) as a white solid. MS: m/e=203.4 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178522B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-20cf030f0bec4b029a833ced77cbe858 |
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| Source note | uspto-grants-2012_05 |
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