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

1,5-Dibromopentane → 2-Amino-5-piperidinomethylpyrrolo[2,3-d]pyrimidin-4-one

HRID 1903312
ノート
印刷プレビュー

反応式

HRID 1903312 の反応式
[NH2:1][C:2]1[N:7]=[C:6]2[N:8]=[CH:9][C:10]([CH2:11][NH2:12])=[C:5]2[C:4](=[O:13])[N:3]=1.Br[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19]Br.[OH-].[Na+]>CO>[NH2:1][C:2]1[N:7]=[C:6]2[N:8]=[CH:9][C:10]([CH2:11][N:12]3[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]3)=[C:5]2[C:4](=[O:13])[N:3]=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 3

HCID 81001,5-DibromopentaneHCID 14798Sodium HydroxideHCID 202463772-Amino-5-aminomethylpyrrolo[2,3-d]pyrimidin-4-one

生成物 1

HCID 204685472-Amino-5-piperidinomethylpyrrolo[2,3-d]pyrimidin-4-one収率 30.6%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

In 4.5 ml of methanol were dissolved 151 mg of 2-amino-5-aminomethylpyrrolo[2,3-d]pyrimidin-4-one (dihydrochloride) and 138 mg of 1,5-dibromopentane, followed by addition of 2.4 ml of 1 N-sodium hydroxide. The mixture was stirred at room temperature for 4 days. The solvent was then distilled off under pressure and the residue was purified by silica gel column chromatography. The fractions containing the desired compound were pooled and after addition of an excess of hydrogen chloride/ethanol, concentrated to dryness, followed by precipitation with ether to give 45 mg of the desired compound.

後処理

  1. distillationThe solvent was then distilled off under pressure
  2. customthe residue was purified by silica gel column chromatography
  3. additionThe fractions containing the desired compound
  4. additionafter addition of an excess of hydrogen chloride/ethanol
  5. concentrationconcentrated to dryness
  6. customfollowed by precipitation with ether

出典と根拠

ORDレコード
ord-0f71452bb0eb40b192ef1df5e3e0df32
出典データセット
uspto-grants-1984_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04435569

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