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

Benzyl Bromide → N-Benzyl-N-(2-bromo-pyridin-3-yl)-4-phenoxy-benzenesulfonamide

HRID 1716279
ノート
印刷プレビュー

反応式

HRID 1716279 の反応式
[Br:1][C:2]1[C:7]([NH:8][S:9]([C:12]2[CH:17]=[CH:16][C:15]([O:18][C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)=[CH:14][CH:13]=2)(=[O:11])=[O:10])=[CH:6][CH:5]=[CH:4][N:3]=1.C([O-])([O-])=O.[K+].[K+].[CH2:31](Br)[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>CN(C=O)C.CCOC(C)=O.O>[CH2:31]([N:8]([C:7]1[C:2]([Br:1])=[N:3][CH:4]=[CH:5][CH:6]=1)[S:9]([C:12]1[CH:17]=[CH:16][C:15]([O:18][C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)=[CH:14][CH:13]=1)(=[O:11])=[O:10])[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 86619931N-(2-Bromo-pyridin-3-yl)-4-phenoxy-benzenesulfonamide

生成物 1

HCID 86619932N-Benzyl-N-(2-bromo-pyridin-3-yl)-4-phenoxy-benzenesulfonamide

試薬・触媒・溶媒 3

HCID 962Water溶媒HCID 6228Dimethylformamide
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

To a suspension of N-(2-bromo-pyridin-3-yl)-4-phenoxy-benzene-sulfonamide (0.38 g, 0.94 mmol) from step A and K2CO3 (0.39 g, 2.81 mmol) in dry DMF (10 mL) was added benzylbromide (0.13 mL, 1.13 mmol). The resulting mixture was heated at 80 C overnight. The cooled reaction was diluted with EtOAc and water. The aqueous layer was extracted with EtOAc (×3) and the combined organics were washed with water and brine, dried over anhydrous Na2SO4, and filtered through Celite. The filtrate was concentrated under the reduced pressure and purified by chromatography (silica gel, 25% EtOAc/hexanes). MS: 495, 497 (M+H)+.

後処理

  1. temperatureThe resulting mixture was heated at 80 C overnight
  2. customThe cooled reaction
  3. extractionThe aqueous layer was extracted with EtOAc (×3)
  4. washthe combined organics were washed with water and brine
  5. dry with materialdried over anhydrous Na2SO4
  6. filtrationfiltered through Celite
  7. concentrationThe filtrate was concentrated under the reduced pressure
  8. custompurified by chromatography (silica gel, 25% EtOAc/hexanes)

出典と根拠

ORDレコード
ord-a5e6b819d4894836bc7d8f888827d806
出典データセット
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07803793B2

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