ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

N-(3-Bromo-6-fluoro-imidazo[1,2-a]pyridin-2-yl)-2,2,2-trifluoro-acetamide → N-(3-cyclopropyl-6-fluoro-imidazo[1,2-a]pyridin-2-yl)-2,2,2-trifluoro-acetamide

HRID 556312
ノート
印刷プレビュー

反応式

HRID 556312 の反応式
[Br-].[CH:2]1([Zn+])[CH2:4][CH2:3]1.Br[C:7]1[N:11]2[CH:12]=[C:13]([F:16])[CH:14]=[CH:15][C:10]2=[N:9][C:8]=1[NH:17][C:18](=[O:23])[C:19]([F:22])([F:21])[F:20]>O1CCCC1.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>[CH:2]1([C:7]2[N:11]3[CH:12]=[C:13]([F:16])[CH:14]=[CH:15][C:10]3=[N:9][C:8]=2[NH:17][C:18](=[O:23])[C:19]([F:22])([F:21])[F:20])[CH2:4][CH2:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 57607463N-(3-Bromo-6-fluoro-imidazo[1,2-a]pyridin-2-yl)-2,2,2-trifluoro-acetamide2 回HCID 178419765HCID 178419765、化合物2 回

生成物 1

HCID 57607458N-(3-cyclopropyl-6-fluoro-imidazo[1,2-a]pyridin-2-yl)-2,2,2-trifluoro-acetamide

試薬・触媒・溶媒 2

HCID 178418397HCID 178418397、化合物触媒2 回
HCID 8028
Tetrahydrofuran
溶媒
3 回

実験手順

Tetrakis(triphenylphosphine)palladium(0) (0.0797 g, 0.000069 mol) was added to a solution of 0.50 M of cyclopropylzinc bromide in tetrahydrofuran (4.1 mL) and N-(3-bromo-6-fluoro-imidazo[1,2-a]pyridin-2-yl)-2,2,2-trifluoro-acetamide (compound d, 0.225 g, 0.000690 mol) in tetrahydrofuran (20.0 mL) and the reaction was heated to reflux for 3 hours. An additional 0.50 M of cyclopropylzinc bromide (4.1 mL) in tetrahydrofuran and tetrakis(triphenylphosphine)palladium(0)(0.080 g) was added and the mixture was heated to reflux overnight. The reaction was concentrated in vacuo and crude product purified by column chromatography (50% ethyl acetate/hexanes) to give N-(3-cyclopropyl-6-fluoro-imidazo[1,2-a]pyridin-2-yl)-2,2,2-trifluoro-acetamide as a yellow solid. Rf 0.46, 50% ethyl acetate/hexanes; MS m/z 287 (M+H).

後処理

  1. temperaturethe reaction was heated
  2. temperatureto reflux for 3 hours
  3. temperaturethe mixture was heated
  4. temperatureto reflux overnight
  5. concentrationThe reaction was concentrated in vacuo and crude product
  6. custompurified by column chromatography (50% ethyl acetate/hexanes)

出典と根拠

ORDレコード
ord-d38e5188f66d48a4b238dde5d3f52ecf
出典データセット
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08058274B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート