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

Cyclopropanecarboxaldehyde → N-(Cyclopropyhnethyl)-N-{2-[4-(3,4-difluorophenoxy)-1-piperidinyl]ethyl}amine

HRID 968761
ノート
印刷プレビュー

反応式

HRID 968761 の反応式
[F:1][C:2]1[CH:3]=[C:4]([CH:15]=[CH:16][C:17]=1[F:18])[O:5][CH:6]1[CH2:11][CH2:10][N:9]([CH2:12][CH2:13][NH2:14])[CH2:8][CH2:7]1.[CH:19]1([CH:22]=O)[CH2:21][CH2:20]1>CO>[CH:19]1([CH2:22][NH:14][CH2:13][CH2:12][N:9]2[CH2:8][CH2:7][CH:6]([O:5][C:4]3[CH:15]=[CH:16][C:17]([F:18])=[C:2]([F:1])[CH:3]=3)[CH2:11][CH2:10]2)[CH2:21][CH2:20]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 123114CyclopropanecarboxaldehydeHCID 693106352-[4-(3,4-Difluorophenoxy)-1-piperidinyl]ethylamine

生成物 1

HCID 70015962N-(Cyclopropyhnethyl)-N-{2-[4-(3,4-difluorophenoxy)-1-piperidinyl]ethyl}amine

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

The product of Step d (0.4 g) dissolved in MeOH (6 ml) was added to cyclopropanecarbaldehyde (0.116 ml) and the resulting mixture was stirred for 4 hours. The solvent was evaporated, the residue re-dissolved in methanol (6 ml) and NaBH4 (0.095 g) added and the mixture left for 30 minutes. Aqueous sodium hydroxide (1N) was added and the aqueous extracted with diethyl ether. The organic extracts were dried with Na2SO4, filtered and concentrated to give the sub-title product as an oil (0.493 g).

後処理

  1. customThe solvent was evaporated
  2. dissolutionthe residue re-dissolved in methanol (6 ml)
  3. additionNaBH4 (0.095 g) added
  4. waitthe mixture left for 30 minutes
  5. additionAqueous sodium hydroxide (1N) was added
  6. extractionthe aqueous extracted with diethyl ether
  7. dry with materialThe organic extracts were dried with Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-331e1f71b3e442c1bc4d25e8a8cec63a
出典データセット
uspto-grants-2007_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07304077B2

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