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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1072000생성일: 2026년 10월 23일

Pyridine → HCID 178440950, 화합물

https://huagongshe.com/ko/reaction/1072000

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물DimethylformamideHCID 6228—
반응물4-tert-Butylbenzyl alcoholHCID 13416—
반응물DiisopropylethylamineHCID 81531—
반응물4-Nitrophenyl chloroformateHCID 82129—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물HCID 178440950HCID 178440950—

반응 단계

To a solution of 4-tert-butylbenzyl alcohol (1.97 g, 12 mmol) in DCM (30 mL) was added pyridine (1.3 mL) and then a solution of 4-nitrophenyl chloroformate (1.57 g, 7.8 mmol) in DCM (20 mL). The mixture was stirred at room temperature for 1 h, concentrated under reduced pressure, and to the residue was added a mixture of of 4,5,6,7-tetrahydromidazo[4,5-c]pyridine (1.5 g, 7 mmol), methanol (3.3 mL), DMF (30 mL), and diisopropylethylamine (4.1 mL). The resulting mixture was stirred at room temperature overnight and concentrated under reduced pressure. The residue was distributed between water and ethyl acetate, phases were separated, and the organic layer was washed with water, dried (MgSO4), and filtered. A solution of oxalic acid (0.63 g) in ethyl acetate was added to the filtrate and the mixture was allowed to stand for 24 h. Filtration yielded the title compound as colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06908926B1
출처 데이터셋uspto-grants-2005_06
ORD IDord-597b2f8d88f84ce8a7442fc7e07d1de4
출처 메모uspto-grants-2005_06