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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1030115생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1030115

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Butyl chloroformateHCID 61140—
반응물Dimethyl-1,3-thiazole-5-carboxylic acidHCID 736488—
반응물HCID 13075762HCID 13075762—
용매TetrahydrofuranHCID 8028—
생성물N-(alpha-cyanofurfuryl)-2,4-dimethylthiazole-5-carboxylic acid amideHCID 1457991363.3%

반응 단계

4.71 g of 2,4-dimethylthiazole-5-carboxylic acid was suspended in 70 ml of tetrahydrofuran, and 6.67 g of triethylamine was added. The mixture was stirred. While it was cooled to -10° to -5° C., 4.10 g of n-butyl chloroformate was added, and the mixture was stirred at this temperature for 30 minutes, and then 4.03 g of alpha-(2-furyl)-alpha-aminoacetonitrile hydrochloride was added. The mixture was stirred at room temperature for 5 hours, and then left to stand overnight. The precipitate was separated by filtration and distilled under reduced pressure to remove the solvent. The residue was purified by silica gel column chromatography. Elution with hexane/ethyl acetate gave 4.20 g (yield 53.6%) 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-ad2cf109e44247f9abf60d9c6d226231
출처 메모uspto-grants-1992_04