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

Water → 9-(3,4-Dimethoxy-benzyl)-2,3-dimethoxy-6,7,8,9-tetrahydro-5-thia-8-aza-benzocycloheptene

HRID 458799
ノート
印刷プレビュー

反応式

HRID 458799 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][C:12]([NH:14][CH2:15][CH2:16][S:17][C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[C:20]([O:26][CH3:27])[CH:19]=2)=O)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].O=P(Cl)(Cl)Cl.[BH4-].[Na+].O>CC#N.C(Cl)Cl.CO>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:6]=[CH:7][C:8]=1[O:9][CH3:10])[CH2:11][CH:12]1[C:23]2[CH:22]=[C:21]([O:24][CH3:25])[C:20]([O:26][CH3:27])=[CH:19][C:18]=2[S:17][CH2:16][CH2:15][NH:14]1
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 962WaterHCID 24813Phosphorus oxychlorideHCID 4311764Sodium borohydrideHCID 184425752-(3,4-Dimethoxy-phenyl)-N-[2-(3,4-dimethoxy-phenylsulfanyl)-ethyl]-acetamide

生成物 1

HCID 184425899-(3,4-Dimethoxy-benzyl)-2,3-dimethoxy-6,7,8,9-tetrahydro-5-thia-8-aza-benzocycloheptene収率 30.4%

試薬・触媒・溶媒 2

HCID 6342
Acetonitrile
溶媒
HCID 21226129Dichloromethane methanol溶媒

反応条件

温度
0 °C

実験手順

To a stirred solution of 2-(3,4-dimethoxy-phenyl)-N-[2-(3,4-dimethoxy-phenylsulfanyl)-ethyl]-acetamide (4.0 g, 10.0 mmol) in dry CH3CN (21 ml), was added POCl3 (2.80 ml, 30.0 mmol). The resulting mixture was stirred at reflux for 3 h under nitrogen. After cooling, the reaction mixture was concentrated in vacuo and the residue was dissolved in MeOH (85 ml). The solution was cooled to 0° C. and NaBH4 (2.7 g, 69.0 mmol) was added portionwise, the resulting pale yellow suspension was stirred at RT for 16 h under nitrogen. The reaction mixture was poured into H2O and extracted three times with CH2Cl2. The combined organic phases were dried over anhydrous MgSO4, filtered and concentrated to give a crude oil. Flash chromatography (CH2Cl2/MeOH: 9/1) gave the title product (1.14 g, 27%) as a viscous brown oil.

後処理

  1. temperatureat reflux for 3 h under nitrogen
  2. temperatureAfter cooling
  3. concentrationthe reaction mixture was concentrated in vacuo
  4. dissolutionthe residue was dissolved in MeOH (85 ml)
  5. stirringthe resulting pale yellow suspension was stirred at RT for 16 h under nitrogen
  6. extractionextracted three times with CH2Cl2
  7. dry with materialThe combined organic phases were dried over anhydrous MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customto give a crude oil

出典と根拠

ORDレコード
ord-7679a0520a214ad8b47b212f5b098c19
出典データセット
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07192950B2

反応ノート

読み込み中…

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