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Triethylamine → N-[5-(5-Cyanopyridin-3-ylethynyl)-2-fluorobenzyl]-methanesulfonamide

HRID 606915
ノート
印刷プレビュー

反応式

HRID 606915 の反応式
C(N(CC)CC)C.Br[C:9]1[CH:10]=[N:11][CH:12]=[C:13]([CH:16]=1)[C:14]#[N:15].[F:17][C:18]1[CH:29]=[CH:28][C:27]([C:30]#[C:31][Si](C)(C)C)=[CH:26][C:19]=1[CH2:20][NH:21][S:22]([CH3:25])(=[O:24])=[O:23].[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1.[Br-].[Zn+2].[Br-].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>[C:14]([C:13]1[CH:16]=[C:9]([C:31]#[C:30][C:27]2[CH:28]=[CH:29][C:18]([F:17])=[C:19]([CH:26]=2)[CH2:20][NH:21][S:22]([CH3:25])(=[O:24])=[O:23])[CH:10]=[N:11][CH:12]=1)#[N:15]
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

8

反応物 4

HCID 8471TriethylamineHCID 7367935-BromonicotinonitrileHCID 2724141Tetrabutylammonium Fluoride2 回HCID 67047541N-(2-Fluoro-5-trimethylsilanylethynylbenzyl)-methanesulfonamide

生成物 1

HCID 67047961N-[5-(5-Cyanopyridin-3-ylethynyl)-2-fluorobenzyl]-methanesulfonamide収率 50.6%

試薬・触媒・溶媒 3

HCID 10421208
Zinc bromide
触媒
HCID 178418397HCID 178418397、化合物触媒
HCID 8028Tetrahydrofuran溶媒3 回

反応条件

温度
60 °C

実験手順

Dissolve zinc (II) bromide (94 mg, 0.36 mmol) in tetrahydrofuran (0.75 mL) and treat with triethylamine (0.20 mL, 1.4 mmol). After 4 min add 5-bromonicotinonitrile (55 mg, 0.30 mmol), N-(2-fluoro-5-trimethylsilanylethynylbenzyl) -methanesulfonamide, (prepared as described in PREPARATION 34), (100 mg, 0.33 mmol) and tetrakis(triphenylphosphine)palladium (0) (17 mg, 0.015 mmol) to the reddish solution. Heat to 60° C. and add a 1 M solution of tetrabutylammonium fluoride (0.36 mL) in tetrahydrofuran. After 1 h add additional 1 M tetrabutylammonium fluoride (0.3 mL) in tetrahydrofuran and stir an additional 30 min. Cool to room temperature and filter through diatomaceous earth washing with ethyl acetate. Purify by silica gel chromatography, eluting with a gradient from 60:40 to 40:60 (7:30 hexanes:dichloromethane):ethyl acetate, to give the title compound as a white crystalline solid (50 mg, 50%).

後処理

  1. temperatureCool to room temperature
  2. filtrationfilter through diatomaceous earth
  3. washwashing with ethyl acetate
  4. customPurify by silica gel chromatography
  5. washeluting with a gradient from 60:40 to 40:60 (7:30 hexanes:dichloromethane)

出典と根拠

ORDレコード
ord-54630c9503d6492ba83d33c0591b1825
出典データセット
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07915424B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート