홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Ethyl Acetate → 5-Bromo-1-(cyclopropylmethyl)-3-methylpyridin-2-one

HRID 518453
노트
인쇄 미리보기

반응식

HRID 518453 반응식
C(=O)([O-])[O-].[K+].[K+].[Br:7][C:8]1[CH:9]=[C:10]([CH3:15])[C:11]([OH:14])=[N:12][CH:13]=1.Br[CH2:17][CH:18]1[CH2:20][CH2:19]1.CC(=O)OCC>CN(C=O)C>[Br:7][C:8]1[CH:9]=[C:10]([CH3:15])[C:11](=[O:14])[N:12]([CH2:17][CH:18]2[CH2:20][CH2:19]2)[CH:13]=1
참가 물질반응 조건실험 절차출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8857Ethyl Acetate2회HCID 11430Potassium CarbonateHCID 81503BromomethylcyclopropaneHCID 178422464HCID 178422464, 화합물

생성물 1

HCID 814220925-Bromo-1-(cyclopropylmethyl)-3-methylpyridin-2-one수율 66%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

반응 조건

온도
70 °C

실험 절차

Potassium carbonate (1.32 g, 9.57 mmol) was added to 5-bromo-3-methyl-2-hydroxypyridine (600 mg, 3.19 mmol) and bromomethylcyclopropane (861 mg, 6.38 mmol) in DMF (6 mL). After heating at 70° C. for 3 h, EA extractive work up and silica gel chromatography (PE: EA=30:110:1), the title compound (510 mg, yield: 66.0%) was obtained as a white solid. 1H NMR: (CDCl3, 400 MHz) δ: 7.39 (d, J=2.0 Hz, 1H), 7.26 (d, J=2.0 Hz, 1H), 3.77 (d, J=6.8 Hz, 2H), 2.15 (s, 3H), 0.65-0.60 (m, 2H), 0.40-0.37 (m, 2H). LCMS: 242.1; 244.1 (M+H)+

출처 및 근거

ORD 기록
ord-2ec8613e3dac4f64a9ada4ba0695d0ea
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09115114B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차출처 및 근거반응 노트