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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15727생성일: 2026년 10월 24일

Triethylamine → 4-chloro-N-(1-diazo-2-oxopentan-3-yl)-N-(pent-1-yn-3-yl)benzenesulfonamide

https://huagongshe.com/ko/reaction/15727

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물DiazomethaneHCID 9550—
반응물Isobutyl chloroformateHCID 62365—
반응물2-(4-chloro-N-(pent-1-yn-3-yl)phenylsulfonamido)-butanoic acidHCID 59342373—
용매Acetic AcidHCID 176—
용매Diethyl EtherHCID 3283—
생성물4-chloro-N-(1-diazo-2-oxopentan-3-yl)-N-(pent-1-yn-3-yl)benzenesulfonamideHCID 72259587—

반응 조건

온도-30 °C

반응 단계

To a solution of the compound 60 (498 mg, 1.45 mmol) in 7.5 mL of Et2O were added sequentially 0.24 mL of triethylamine (1.2 eq), 0.23 mL of isobutyl chloroformate (1.2 eq) at −30° C. After being stirred at −30° C. for 15 min, diazomethane (prepared by mixing MNNG and KOH in diethyl ether) (excess) was added to the above mixture at 0° C. and stirred there for 5 hours. Glacial HOAc (1.5 mL) was added to destroy the excess diazomethane and the solution was extracted with EtOAc. The organic phase was washed with sat NaHCO3, water, brine and dried (MgSO4). LCMS 368.1 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732609B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c6a04bb7504c4ce18d8cc8e65ca5dd39
출처 메모uspto-grants-2010_06