돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 336546생성일: 2026년 10월 25일

Diisopropylethylamine → Ethyl 5-[2-(6-Fluoroquinolin-2-yl)-2-azaspiro[3.3]hept-6-ylcarbamoyloxymethyl]isoxazole-3-carboxylate

https://huagongshe.com/reaction/336546

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2-Chloro-6-fluoroquinolineHCID 15059433—
반응물Ethyl 5-(2-azaspiro[3.3]hept-6-ylcarbamoyloxymethyl)isoxazole-3-carboxylate trifluoroacetateHCID 68000734—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물Ethyl 5-[2-(6-Fluoroquinolin-2-yl)-2-azaspiro[3.3]hept-6-ylcarbamoyloxymethyl]isoxazole-3-carboxylateHCID 68000144—

반응 단계

The process is performed according to the procedure described in Example 2 (step 2.6.). Starting with 0.43 g (1.03 mmol) of ethyl 5-(2-azaspiro[3.3]hept-6-ylcarbamoyloxymethyl)isoxazole-3-carboxylate trifluoroacetate, obtained in step 11.8., 0.187 g (1.03 mmol) of 2-chloro-6-fluoroquinoline and 0.399 g (3.09 mmol) of N,N-diisopropylethylamine, and after chromatography on silica gel, eluting with a 98/2 mixture of dichloromethane and methanol, 0.15 g of pure product in the form of a beige-coloured solid is thus obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889702B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-3bcf12f5201843a29d4239b248f9fbcc
출처 메모uspto-grants-2014_11