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

2-Bromo-6-(fluoromethyl)pyridine → HCID 66598150, 화합물

HRID 422492
노트
인쇄 미리보기

반응식

HRID 422492 반응식
Br[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8][F:9])[N:3]=1.[CH2:10]([C:14]1[N:15]=[C:16]2[CH:21]=[CH:20][C:19]([F:22])=[CH:18][N:17]2[CH:23]=1)[CH2:11][C:12]#[CH:13]>>[F:22][C:19]1[CH:20]=[CH:21][C:16]2[N:17]([CH:23]=[C:14]([CH2:10][CH2:11][C:12]#[C:13][C:2]3[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8][F:9])[N:3]=3)[N:15]=2)[CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 102416102-Bromo-6-(fluoromethyl)pyridineHCID 860867362-(But-3-ynyl)-6-fluoro-imidazo[1,2-a]pyridine

생성물 1

HCID 66598150HCID 66598150, 화합물

실험 절차

The title compound was prepared in accordance with the general method of Example 190(F), from 2-bromo-6-(fluoromethyl)pyridine (220 mg, 1.10 mmol) and 2-(but-3-ynyl)-6-fluoro-imidazo[1,2-a]pyridine (220 mg, 1.14 mmol). The crude residue was purified over C18 chromatography (prepacked 35 g silicagel column, H2O/CH3CN: from 95/5 to 55/45 as eluent) to afford 1.55 mg of 6-fluoro-2-(4-(6-(fluoromethyl)pyridin-2-yl)but-3-ynyl)H-imidazo[1,2-a]pyridine (Yield: 46%) as a white powder (Mp=140-141.8° C.).

후처리

  1. customThe crude residue was purified over C18 chromatography (prepacked 35 g silicagel column, H2O/CH3CN: from 95/5 to 55/45 as eluent)

출처 및 근거

ORD 기록
ord-9ff32e9558024cfc83598690142dc41a
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08101637B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트