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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1030112생성일: 2026년 10월 27일

Triethylamine → N-(alpha-cyanofurfuryl)-2,4-dimethylthiazole-5-carboxylic acid amide

https://huagongshe.com/reaction/1030112

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Triethylamine hydrochlorideHCID 11130—
반응물2-Furanacetonitrile, alpha-amino-HCID 11147706—
반응물2,4-Dimethylthiazole-5-carbonyl chlorideHCID 14653140—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물N-(alpha-cyanofurfuryl)-2,4-dimethylthiazole-5-carboxylic acid amideHCID 1457991390%

반응 단계

In 120 ml of ethylacetate were dissolved 6.2 g of alpha-(2-furyl)-alpha-aminoacetonitrile and 6.0 g of triethylamine, and with stirring, the 2,4-dimethylthiazole5-carboxylic acid chloride was added dropwise to the solution, and the mixture was stirred at room temperature for 1 hour. Water (150 ml) was added, and the precipitated triethylamine hydrochloride was dissolved. The ethyl acetate layer was separated, washed with water, and dried over sodium sulfate. The dried ethyl acetate layer was distilled under reduced pressure to remove the solvent. The residue was recrystallized from isopropyl ether to give 11.65 g (yield 90.0%) of the desired N-(alpha-cyanofurfuryl)-2,4-dimethylthiazole-5-carboxylic acid amide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05104886
출처 데이터셋uspto-grants-1992_04
ORD IDord-eb2400d6d07f40b39555abfe687e9fa6
출처 메모uspto-grants-1992_04