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

(1R,2S)-Tranylcypromine → HCID 58842375、化合物

HRID 1270443
ノート
印刷プレビュー

反応式

HRID 1270443 の反応式
[CH2:1]1[C@@H:3]([NH2:4])[C@@H:2]1[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[N:11]([CH:14]([CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[C:15]([O:17]CC)=O)=[C:12]=[O:13]>ClCCl>[CH2:20]([CH:14]1[NH:11][C:12](=[O:13])[N:4]([CH2:3][C:2]2([C:5]3[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=3)[CH2:1][CH2:5][CH2:2][CH2:1][CH2:3]2)[C:15]1=[O:17])[C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=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 19493(1R,2S)-TranylcypromineHCID 12370705Ethyl N-(oxomethylidene)phenylalaninate

生成物 1

HCID 58842375HCID 58842375、化合物収率 38.5%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A solution of compound 1 (0.255 g; 1.35 mmol) in anhydrous dichloromethane (8 mL) was treated with ethyl 2-isocyanato-3-phenylpropionate (0.325 g; 0.38 mmol) and stirred at room temperature overnight. The solvent was removed by evaporation, the residue was dissolved in ethanol (1 mL), 6N hydrochloric acid (0.5 mL) and water (0.5 mL) and the reaction mixture was heated to 50° C. After 3 h at 50° C., additional 6N hydrochloric acid (1 mL) was added and the reaction mixture was heated at 65° C. overnight. The reaction mixture was concentrated and the crude product was purified directly by column chromatography on silica gel using 1:1 ethyl acetate:hexane as the eluent to give 0.053 g of 5-Benzyl-3-(1-phenyl-cyclohexylmethyl)-imidazolidine-2,4-dione as a white solid. Mass Spec [M+H]+=363.

後処理

  1. customThe solvent was removed by evaporation
  2. dissolutionthe residue was dissolved in ethanol (1 mL)
  3. temperature6N hydrochloric acid (0.5 mL) and water (0.5 mL) and the reaction mixture was heated to 50° C
  4. waitAfter 3 h at 50° C.
  5. additionadditional 6N hydrochloric acid (1 mL) was added
  6. temperaturethe reaction mixture was heated at 65° C. overnight
  7. concentrationThe reaction mixture was concentrated
  8. customthe crude product was purified directly by column chromatography on silica gel using 1:1 ethyl acetate

出典と根拠

ORDレコード
ord-8ca88ec8d5c94c61bb35106fd54c435b
出典データセット
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07202253B2

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