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

2,4-Diamino-5-(1,2,3,4-tetrahydro-8-methoxy-6-quinolylmethyl)pyrimidine → 5-[(8-Methoxyquinolin-6-yl)methyl]pyrimidine-2,4-diamine

HRID 279979
ノート
印刷プレビュー

反応式

HRID 279979 の反応式
[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([CH2:9][C:10]2[CH:11]=[C:12]3[C:17](=[C:18]([O:20][CH3:21])[CH:19]=2)[NH:16][CH2:15][CH2:14][CH2:13]3)=[CH:4][N:3]=1>[Pd].C1(C(C)C)C=CC=CC=1>[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([CH2:9][C:10]2[CH:11]=[C:12]3[C:17](=[C:18]([O:20][CH3:21])[CH:19]=2)[N:16]=[CH:15][CH:14]=[CH:13]3)=[CH:4][N:3]=1
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 233230562,4-Diamino-5-(1,2,3,4-tetrahydro-8-methoxy-6-quinolylmethyl)pyrimidine

生成物 1

HCID 233230575-[(8-Methoxyquinolin-6-yl)methyl]pyrimidine-2,4-diamine

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 7406Cumene溶媒

反応条件

温度
150 °C

実験手順

The product of Example 2 was oxidised using 20% palladium on charcoal in 50 ml of cumene, by heating at 150° C. for 21 hours. After the catalyst was removed and the solvent evaporated, the residue was purified on a silica gel column which was eluted with methylene chloride:methanol/19:1. This produced 0.51 g (35%) of the title compound, which melted at 285°-287° after recrystallisation from betamethoxyethanol. Anal. Calcd. for C15H15N5O: C, 64.04; H, 5.37; N, 24.89. Found: C, 63.88; H, 5.37; N, 24.84.

後処理

  1. customAfter the catalyst was removed
  2. customthe solvent evaporated
  3. customthe residue was purified on a silica gel column which
  4. washwas eluted with methylene chloride
  5. customThis produced 0.51 g (35%) of the title compound, which melted at 285°-287° after recrystallisation from betamethoxyethanol

出典と根拠

ORDレコード
ord-1992c08263a54b7e8082bb60778c5538
出典データセット
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04587341

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート