돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 336528생성일: 2026년 10월 25일

Diisopropylethylamine → HCID 68000123, 화합물

https://huagongshe.com/reaction/336528

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4-Nitrophenyl chloroformateHCID 82129—
반응물Ethyl 5-(hydroxymethyl)isoxazole-3-carboxylateHCID 8027233—
반응물tert-Butyl 2-amino-6-azaspiro[3.4]octane-6-carboxylateHCID 56962195—
용매1,2-DichloroethaneHCID 11—
용매WaterHCID 962—
생성물HCID 68000123HCID 6800012373.9%

반응 조건

온도0 °C

반응 단계

A solution of 0.304 g (1.51 mmol) of 4-nitrophenyl chloroformate dissolved in 5 mL of 1,2-dichloroethane is added dropwise to a solution containing 0.284 g (1.66 mmol) of ethyl 5-hydroxymethylisoxazole-3-carboxylate and 0.39 g (3.02 mmol) of N,N-diisopropylethylamine in 10 mL of 1,2-dichloroethane, cooled to about 0° C. Stirring is continued at 0° C. for 1 hour and then at room temperature for 1 hour. 0.39 g (3.02 mmol) of N,N-diisopropylethylamine and then 0.34 g (1.51 mmol) of tert-butyl 2-amino-6-azaspiro[3.4]octane-6-carboxylate, prepared in step 6.4., are added. The reaction medium is stirred at 70° C. for 4 hours. It is allowed to cool to room temperature. Water is added to the reaction medium, the aqueous phase is separated out and extracted several times with dichloromethane, the combined organic phases are washed with aqueous sodium hydroxide solution (1N) and then with saturated aqueous ammonium chloride solution and dried over sodium sulfate, and the filtrate is concentrated under reduced pressure. 0.44 g of pure product is thus obtained in the form of an orange oil, which is used without further purification in the following step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889702B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-c3524bda5e0d4f5b8b9a9cb08c4392a6
출처 메모uspto-grants-2014_11