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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2376069생성일: 2026년 10월 25일

Hydrochloric Acid → ethyl 6-{[(3R)-1-(tert-butoxycarbonyl)-3-piperidinyl]amino}-5-chloronicotinate

https://huagongshe.com/reaction/2376069

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DiisopropylethylamineHCID 81531—
반응물tert-butyl (3R)-3-aminopiperidine-1-carboxylateHCID 1501974—
반응물Ethyl 5,6-DichloronicotinateHCID 16762519—
용매WaterHCID 962—
용매1,3-Dimethyl-2-imidazolidinoneHCID 6661—
용매Ethyl AcetateHCID 8857—
생성물ethyl 6-{[(3R)-1-(tert-butoxycarbonyl)-3-piperidinyl]amino}-5-chloronicotinateHCID 68960873—

반응 조건

온도100 °C

반응 단계

To a solution of ethyl 5,6-dichloronicotinate (10.0 g) and N,N-diisopropylethylamine (17.4 mL) in 1,3-dimethyl-2-imidazolidinone (100 mL) was added tert-butyl (3R)-3-amino-1-piperidinecarboxylate (10.9) at ambient temperature and the mixture was stirred at 100° C. for 9 hr. The reaction mixture was poured into a mixture of AcOEt and water. The separated organic layer was added ice-water and the mixture was adjusted to pH 3.5 with 1N-HCl. The separated organic layer was washed with water, dried over magnesium sulfate and evaporated in vacuo to give ethyl 6-{[(3R)-1-(tert-butoxycarbonyl)-3-piperidinyl]amino}-5-chloronicotinate (16.74 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07465731B2
출처 데이터셋uspto-grants-2008_12
ORD IDord-11bc7f4dde0446e7a736587afcaa09bb
출처 메모uspto-grants-2008_12