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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1614907생성일: 2026년 10월 25일

Diisopropylethylamine → HCID 178499337, 화합물

https://huagongshe.com/reaction/1614907

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물3-(3-Benzyloxy-cyclobutylamino)-5-(3,3-dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid methyl esterHCID 58113975—
반응물HCID 178461265HCID 178461265—
반응물HCID 178499338HCID 178499338—
용매1,2-DichloroethaneHCID 11—
생성물HCID 178499337HCID 178499337—

반응 조건

온도100 °C

반응 단계

A mixture of 3-(3-Benzyloxy-cyclobutylamino)-5-(3,3-dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid methyl ester (1.26 g, 3.17 mmol) and N,N-diisopropylethylamine (2.4 mL, 13.8 mmol) in DCE (8 mL) was treated with trans-4-methyl-cyclohexanecarbonyl chloride and heated to 100° C. for 5 hours. The reaction mixture was cooled to room temperature, adsorbed onto silica, and purified by silica gel chromatography (0-30% ethyl acetate:hexanes). This resulted in 590 mg (36% yield) of cis-cyclobutyl isomer (cis-3-[(3-benzyloxy-cyclobutyl)-(4-methyl-cyclohexanecarbonyl)-amino]-5-(3,3-dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid methyl ester) and 230 mg (14% yield) of the trans-cyclobutyl isomer (trans-3-[(3-benzyloxy-cyclobutyl)-(4-methyl-cyclohexanecarbonyl)-amino]-5-(3,3-dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid methyl ester).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08765722B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-29799bc22e1147ee93d830ce75c64fd6
출처 메모uspto-grants-2014_07