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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
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(3-Dibenzylamino-2-hydroxy-5-methyl-hexyl)-phosphonic acid dimethyl ester → Phosphonic acid, P-(3-amino-2-hydroxy-5-methylhexyl)-, dimethyl ester

HRID 1923459
ノート
印刷プレビュー

反応式

HRID 1923459 の反応式
[CH3:1][O:2][P:3]([CH2:7][CH:8]([OH:29])[CH:9]([N:14](CC1C=CC=CC=1)CC1C=CC=CC=1)[CH2:10][CH:11]([CH3:13])[CH3:12])(=[O:6])[O:4][CH3:5]>CO.[C].[Pd]>[CH3:1][O:2][P:3]([CH2:7][CH:8]([OH:29])[CH:9]([NH2:14])[CH2:10][CH:11]([CH3:12])[CH3:13])(=[O:6])[O:4][CH3:5]
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

4

反応物 1

HCID 72266810(3-Dibenzylamino-2-hydroxy-5-methyl-hexyl)-phosphonic acid dimethyl ester

生成物 1

HCID 72266813Phosphonic acid, P-(3-amino-2-hydroxy-5-methylhexyl)-, dimethyl ester

試薬・触媒・溶媒 2

HCID 178418390HCID 178418390、化合物触媒HCID 887Methanol溶媒

反応条件

温度
39.5 °C

実験手順

Reaction 4: A diastereomeric mixture of the crude (3-dibenzylamino-2-hydroxy-5-methyl-hexyl)-phosphonic acid dimethyl ester, compound 4, obtained in reaction 3, was treated with palladium-carbon (2.0% wt) as the catalyst in methanol (40 mL). The mixture reaction was stirred for 12 h under a hydrogen gas atmosphere at 37-42° C., and after this period of time, the mixture was filtered through a pad of Celite, and the solvents were removed under reduced pressure to leave (3-amino-2-hydroxy-5-methyl-hexyl)-phosphonic acid dimethyl ester, compound 5, as a crude oil.

後処理

  1. customReaction 4
  2. customobtained in reaction 3
  3. customThe mixture reaction
  4. waitafter this period of time
  5. filtrationthe mixture was filtered through a pad of Celite
  6. customthe solvents were removed under reduced pressure

出典と根拠

ORDレコード
ord-6b00c811db4544c9ad36cfa569e96ba8
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08178515B2

反応ノート

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