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

Nitrogen → 2-Fluoro-5-(thiazol-2-yl)benzonitrile

HRID 1891446
노트
인쇄 미리보기

반응식

HRID 1891446 반응식
Br[C:2]1[S:3][CH:4]=[CH:5][N:6]=1.[C:7]([C:9]1[CH:10]=[C:11](B(O)O)[CH:12]=[CH:13][C:14]=1[F:15])#[N:8].C([O-])([O-])=O.[K+].[K+].N#N>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.COCCOC.O>[F:15][C:14]1[CH:13]=[CH:12][C:11]([C:2]2[S:3][CH:4]=[CH:5][N:6]=2)=[CH:10][C:9]=1[C:7]#[N:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 947NitrogenHCID 11430Potassium CarbonateHCID 764302-BromothiazoleHCID 27579643-Cyano-4-fluorophenylboronic acid

생성물 1

HCID 583671252-Fluoro-5-(thiazol-2-yl)benzonitrile수율 71%

시약·촉매·용매 2

HCID 178418397
HCID 178418397, 화합물
촉매
HCID 18180031Water 1,2-dimethoxyethane용매

반응 조건

온도
85 °C

실험 절차

A solution of 2-bromothiazole (25 g, 153.4 mmol), (3-cyano-4-fluorophenyl)boronic acid (25.3 g, 153.3 mmol), K2CO3 (63.6 g, 460 mmol) and 3:1 DME/H2O (205 mL) was purged with N2 for 1 h before the addition of Pd(PPh3)4 (9.2 g, 7.9 mmol). The mixture was further degassed with N2 for 5 min and then heated to 85° C. for 7 h under N2. Upon cooling, the reaction mixture was diluted with EA (250 mL), washed with water (200 mL) and brine (200 mL), and dried over MgSO4. The reaction mixture was filtered and concentrated to give beige solid. The crude product was purified by recrystallization from 20% EA/hexanes to afford 22 g (71%) of 2-fluoro-5-(thiazol-2-yl)benzonitrile THZ INT-1 as a pale yellow solid. LCMS-ESI (m/z) calculated for C10H5FN2S: 204.2; found 205.0 [M+H]+, tR=3.26 min. 1H NMR (400 MHz, CDCl3) δ 8.21-8.16 (m, 1H), 8.15-8.08 (m, 1H), 7.86-7.81 (m, 1H), 7.36-7.32 (m, 1H), 7.27-7.21 (m, 1H). 13C NMR (101 MHz, CDCl3) δ 164.31, 162.22, 143.73, 132.68, 131.28, 128.34, 119.94, 116.98, 113.10.

후처리

  1. customThe mixture was further degassed with N2 for 5 min
  2. temperatureUpon cooling
  3. additionthe reaction mixture was diluted with EA (250 mL)
  4. washwashed with water (200 mL) and brine (200 mL)
  5. dry with materialdried over MgSO4
  6. filtrationThe reaction mixture was filtered
  7. concentrationconcentrated
  8. customto give beige solid
  9. customThe crude product was purified by recrystallization from 20% EA/hexanes

출처 및 근거

ORD 기록
ord-072563af10114a148169a8008480606f
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507538B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트