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

Potassium Hydroxide → L-Phenylalanine

HRID 2254285
ノート
印刷プレビュー

反応式

HRID 2254285 の反応式
C[O:2][C:3](=[O:33])[C@H:4]([CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[NH:5]C(CC1N(CC2C=CC=CC=2Cl)C(SCCC)=NC=1)=O.[OH-].[K+]>C(O)C.O>[NH2:5][C@H:4]([C:3]([OH:33])=[O:2])[CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=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 14797Potassium HydroxideHCID 54145803N-[{1-(2-chlorophenyl)methyl-2-propylthio-1H-imidazol-5-yl}methylcarbonyl]-L-phenylalanine methyl ester

生成物 1

HCID 6140L-Phenylalanine

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

The methyl ester from Example 9 (i) (0.58 g, 1.2 mmol) was dissolved in ethanol (10 mL) and a solution of potassium hydroxide (0.223 g, 4 mmol) in water (4 mL) was added. This solution was stirred at room temperature for 1.5 hours. The ethanol was evaporated, the residue was diluted with water (10 mL) and the basic solution was extracted with ether. The aqueous layer was acidified to pH 3.5 with 10% hydrochloric acid solution, and the cooled suspension was then filtered, washed with water and dried in vacuum to provide 0.46 g (82%) of N-[1-(2-chlorophenyl)methyl-2-propylthio-1H-imidazol-5-yl}methylcarbonyl]-L-phenylalanine; mp 120°-121° C.

後処理

  1. customThe ethanol was evaporated
  2. additionthe residue was diluted with water (10 mL)
  3. extractionthe basic solution was extracted with ether
  4. filtrationthe cooled suspension was then filtered
  5. washwashed with water
  6. customdried in vacuum

出典と根拠

ORDレコード
ord-5a3f3693207a458b910f049270af9f40
出典データセット
uspto-grants-1993_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05234917

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