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

HRID 1891446
ノート
印刷プレビュー

反応式

HRID 1891446 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 178418397
HCID 178418397、化合物
触媒
HCID 18180031Water 1,2-dimethoxyethane溶媒

反応条件

温度
85 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-072563af10114a148169a8008480606f
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08507538B2

反応ノート

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