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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2355900생성일: 2026년 10월 25일

Methyl 2-(bis((tert-butoxy)carbonyl)amino)prop-2-enoate → 2-(Di-tert-butoxycarbonylamino)-3-(7,7-dimethyl-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl)-propionic acid methyl ester

https://huagongshe.com/reaction/2355900

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 2-(bis((tert-butoxy)carbonyl)amino)prop-2-enoateHCID 10870342—
반응물7,7-dimethyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridineHCID 21102209—
용매MethanolHCID 887—
생성물2-(Di-tert-butoxycarbonylamino)-3-(7,7-dimethyl-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl)-propionic acid methyl esterHCID 58864404—

반응 단계

To a solution of 7,7-dimethyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine (160 mg) in methanol (3 mL) was added 2-(di-tert-butoxycarbonylamino)-acrylic acid methyl ester (331 mg). A gentle stream of nitrogen was applied and the reaction stirred overnight. In the morning, the volume was greatly reduced. The last traces of solvent were removed under high vacuum to give 490 mg (quant.) which was used without purification. 1H-NMR (CDCl3, 500 MHz) δ 1.24 (s, 3H), 1.26 (s, 3H), 1.38 (s, 18H), 2.33 (d, J=11.3, 1H), 2.57 (d, J=11.3, 1H), 3.09 (dd, J=13.1, 5.5, 1H), 3.15 (dd, J=13.4, 9.5, 1H), 3.35 (d, J=12.8, 1H), 3.57 (d, J=12.8, 1H), 3.68 (s, 3H), 5.13 (dd, J=9.5, 3.7, 1H), 7.16 (s, 1H). Mass spec.: 453.30 (MH)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07754732B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-f3e84e54c65e4a74a0fe4b989151a7e9
출처 메모uspto-grants-2010_07