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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2188583생성일: 2026년 10월 25일

1,3-Benzodioxole-5-carbonyl chloride → Benzo[1,3]dioxole-5-carboxylic acid (4-{3-[2-(3-trifluoromethyl-benzoylamino)-acetylamino]-azetidin-1-yl}-cyclohexyl)-amide

https://huagongshe.com/reaction/2188583

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Benzodioxole-5-carbonyl chlorideHCID 2734749—
반응물N-{[1-(4-Amino-cyclohexyl)-azetidin-3-ylcarbamoyl]-methyl}-3-trifluoromethyl-benzamide TFA saltHCID 86646662—
용매DichloromethaneHCID 6344—
생성물Benzo[1,3]dioxole-5-carboxylic acid (4-{3-[2-(3-trifluoromethyl-benzoylamino)-acetylamino]-azetidin-1-yl}-cyclohexyl)-amideHCID 49763337—

반응 단계

Benzo[1,3]dioxole-5-carbonyl chloride (Aldrich, 74 mg, 0.404 mmol) was added into a solution of N-{[1-(4-amino-cyclohexyl)-azetidin-3-ylcarbamoyl]-methyl}-3-trifluoromethyl-benzamide TFA salt (as prepared in the previous step 200 mg, 0.404 mmol) and TEA (170 μL, 1.21 mmol) in DCM (5 mL) at 0° C. The reaction was stirred for an additional 2 hours and quenched with saturated sodium bicarbonate. The reaction was then partitioned between DCM and water. The organic layer was separated and the aqueous layer was extracted 3 times with a chloroform/IPA “cocktail” (˜3:1, v/v). The combined organic layer was dried over anhydrous Na2SO4, filtered and concentrated to give the crude product, which was then purified by a CombiFlash® system using ethyl acetate and 7N NH3 in MeOH as eluent (from pure ethyl acetate to 5% 7N NH3 in MeOH in ethyl acetate) to afford the title compound as white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08324186B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-96d423cb081e4ff3b151feca3af765ac
출처 메모uspto-grants-2012_12