HCID 86608383、化合物 → HCID 68517032、化合物

HRID 882751ノート

反応式

HRID 882751 の反応式
[N:1]([C:4]1[N:9]=[C:8]([N:10]2[CH2:15][CH2:14][O:13][CH2:12][CH2:11]2)[N:7]=[C:6]([O:16][CH2:17][C:18]([CH3:21])([OH:20])[CH3:19])[CH:5]=1)=[N+]=[N-]>O1CCCC1.CO.[Pd]>[NH2:1][C:4]1[N:9]=[C:8]([N:10]2[CH2:15][CH2:14][O:13][CH2:12][CH2:11]2)[N:7]=[C:6]([O:16][CH2:17][C:18]([CH3:21])([OH:20])[CH3:19])[CH:5]=1

参加物

5

反応物 1

HCID 86608383HCID 86608383、化合物

生成物 1

HCID 68517032HCID 68517032、化合物

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

1-(6-azido-2-morpholin-4-yl-pyrimidin-4-yloxy)-2-methyl-propan-2-ol was dissolved in a mixture of tetrahydrofuran (200 mL) and methanol (20 mL). To the solution was added 10% palladium on carbon (2 g) and the reaction was stirred under an atmosphere of hydrogen for 24 hours. The reaction was then filtered through celite and evaporated to give 1-(6-amino-2-morpholin-4-yl-pyrimidin-4-yloxy)-2-methyl-propan-2-ol (2.0 g).

後処理

  1. filtrationThe reaction was then filtered through celite
  2. customevaporated

出典と根拠

ORDレコード
ord-47955d7c1dd74d03be43f5c92e5c30e1
出典データセット
uspto-grants-2012_08
特許番号
US08236795B2

反応ノート

読み込み中…