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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2041719생성일: 2026년 10월 27일

Pyridine → [(cis)-1-Acetyl-6-bromo-2-propyl-1,2,3,4-tetrahydro-4-quinolinyl]formamide

https://huagongshe.com/reaction/2041719

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Acetyl chlorideHCID 6367—
반응물[(cis)-6-Bromo-2-propyl-1,2,3,4-tetrahydro-4-quinolinyl]formamideHCID 86669448—
용매DichloromethaneHCID 6344—
생성물[(cis)-1-Acetyl-6-bromo-2-propyl-1,2,3,4-tetrahydro-4-quinolinyl]formamideHCID 8666944768%

반응 단계

[(cis)-6-Bromo-2-propyl-1,2,3,4-tetrahydro-4-quinolinyl]formamide (for a preparation see intermediate 89) (8.0 g, 26.9 mmol) in DCM (100 mL) was added dropwise at room temperature to a mixture of acetyl chloride (6.7 mL, 94.28 mmol) and pyridine (10.85 mL, 134.7 mmol) in DCM (150 mL). The resulting mixture was stirred at this temperature for 1 h then was washed with 1M NaOH aqueous solution, 1M HCl aqueous solution, a saturated NaHCO3 aqueous solution then brine, was dried over MgSO4 and concentrated in vacuovacuo. Purification of the residue by flash chromatography on silica gel (20:1 DCM/MeOH) gave [(cis)-1-acetyl-6-bromo-2-propyl-1,2,3,4-tetrahydro-4-quinolinyl]formamide (6.29 g, 18.5 mmol, 68%) as a light orange solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08580957B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-c53f52c985634eee9c41dc773763c218
출처 메모uspto-grants-2013_11