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

2-Bromo-6-methylpyridine → 4-(6-Methylpyridin-2-yl)-1-naphthoic acid

HRID 352361
노트
인쇄 미리보기

반응식

HRID 352361 반응식
C[Sn](C)(C)[C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]([C:13]([O:15]C)=[O:14])=[CH:5][CH:4]=1.Br[C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([CH3:26])[N:21]=1>>[CH3:26][C:22]1[N:21]=[C:20]([C:3]2[C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[C:6]([C:13]([OH:15])=[O:14])=[CH:5][CH:4]=2)[CH:25]=[CH:24][CH:23]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 792052-Bromo-6-methylpyridineHCID 22711864Methyl 4-(trimethylstannyl)-1-naphthoate

생성물 1

HCID 227118464-(6-Methylpyridin-2-yl)-1-naphthoic acid

실험 절차

The title compound was prepared from D7 and 2-bromo-6-methylpyridine using a similar method to Description 8 (45%), followed by hydrolysis of the methyl ester using 1M NaOH solution (69%) to afford a white solid.

후처리

  1. customto afford a white solid

출처 및 근거

ORD 기록
ord-0a95f086280d451b9d311771a522dfab
출처 데이터셋
uspto-grants-2004_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06747030B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트