돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 536098생성일: 2026년 10월 25일

Acetic Acid → Ethyl 3-[(1H-benzimidazol-2-ylmethyl)amino]-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/536098

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물1H-Benzimidazole-2-carboxaldehydeHCID 76826—
반응물Ethyl 3-amino-1H-pyrrole-2-carboxylateHCID 2773439—
반응물Sodium cyanoborohydrideHCID 5003444—
용매MethanolHCID 887—
생성물Ethyl 3-[(1H-benzimidazol-2-ylmethyl)amino]-1H-pyrrole-2-carboxylateHCID 6706852681.1%

반응 단계

A reaction mixture of 3-amino-1H-pyrrole-2-carboxylic acid ethyl ester (0.77 g, 4.99 mmol), 1H-benzoimidazole-2-carboxaldehyde (0.88 g, 5.99 mmol), NaCNBH3 (0.31 g, 4.99 mmol) and HOAc (0.57 mL, 9.99 mmol) in methanol (15 mL) was stirred at r.t. overnight. The mixture was then heated at 50° C. for 5 h. Cooled to r.t. and evaporated in vacuo. The residue was dissolved in ethyl acetate and washed with water. The aqueous phase was extracted with ethyl acetate (twice). The combined organic layers were dried (MgSO4) and concentrated. The crude product was purified by flash column chromatography (heptane/ethyl acetate (1:0 to 0:1), obtaining 1.15 g (81%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859568B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-6b5f3f91fcb74e599bb6787659d0c083
출처 메모uspto-grants-2014_10