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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 899059생성일: 2026년 10월 23일

2-(2-tert-Butoxycarbonylamino-pyridin-4-ylmethylene)-succinic acid 4-benzyl ester 1-tert-butyl ester → 2-(2-Tert-butoxycarbonylamino-pyridin-4-ylmethyl)-succinic acid 1-tert-butyl ester

https://huagongshe.com/ko/reaction/899059

반응식

참여 물질

역할이름HCID투입량
반응물2-(2-tert-Butoxycarbonylamino-pyridin-4-ylmethylene)-succinic acid 4-benzyl ester 1-tert-butyl esterHCID 54209259—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물2-(2-Tert-butoxycarbonylamino-pyridin-4-ylmethyl)-succinic acid 1-tert-butyl esterHCID 6930298583%

반응 단계

2-(2-tert-Butoxycarbonylamino-pyridin-4-ylmethylene)-succinic acid 4-benzyl ester 1-tert-butyl ester (2.81 g, 7.60 mmol) and Pd/C (10%, 400 mg) were suspended in EtOH and hydrogenated at 41 atm. and 28° C. for 3 days. The catalyst was removed from the reaction mixture by filtration. The catalyst was washed with EtOH (96%). 1 M K2CO3 (30 mL) was added to the filtrate followed by addition of water (50 mL). After 2 days the reaction mixture was evaporated to ca 80 mL, then brine (10 mL) was added and the reaction mixture extracted with ether. The aqueous phase was acidified to pH=3 and extracted with chloroform. Methanol (25 mL) was added and the reaction mixture was dried (Na2SO4+CaSO4) and filtered to give 2-(2-tert-butoxycarbonylamino-pyridin-4-ylmethyl)-succinic acid 1-tert-butyl ester (1.90 g, 83%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07354895B1
출처 데이터셋uspto-grants-2008_04
ORD IDord-7f8f1cafed2747709f9692ed7b1bdb9f
출처 메모uspto-grants-2008_04