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

(4,6-Dibromopyrimidin-2-yl)-methylamine → (4-Bromo-6-phenylsulphanylpyrimidin-2-yl)-methylamine

HRID 1603545
ノート
印刷プレビュー

反応式

HRID 1603545 の反応式
[Br:1][C:2]1[CH:7]=[C:6](Br)[N:5]=[C:4]([NH:9][CH3:10])[N:3]=1.[Na].[C:12]1([SH:18])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>CN1CCCC1=O>[Br:1][C:2]1[CH:7]=[C:6]([S:18][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[N:5]=[C:4]([NH:9][CH3:10])[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

4

反応物 2

HCID 19605496(4,6-Dibromopyrimidin-2-yl)-methylamineHCID 66586497Sodium benzenethiol

生成物 1

HCID 19605540(4-Bromo-6-phenylsulphanylpyrimidin-2-yl)-methylamine収率 65.3%

試薬・触媒・溶媒 1

HCID 13387N-methyl-2-pyrrolidone溶媒

実験手順

0.33 g (0.00124 mol) of (4,6-dibromopyrimidin-2-yl)-methylamine and 0.33 g (0.00248 mol) of thiophenol sodium salt were stirred in 15 ml of 1-methyl-2-pyrrolidone at 120° C. for 4 hrs. The solvent was removed and the residue was partitioned between water and diethyl ether. The ether phase was washed with sat. sodium chloride solution and dried over MgSO4. After filtration and removal of the solvent the residue was chromatographed on silica gel with diethyl ether/hexane 1:3 and subsequently dried in a high vacuum. There was obtained 0.24 g (65%) of (4-bromo-6-phenylsulphanylpyrimidin-2-yl)-methylamine as white crystals; m.p.: 122-124° C.

後処理

  1. customThe solvent was removed
  2. customthe residue was partitioned between water and diethyl ether
  3. washThe ether phase was washed with sat. sodium chloride solution
  4. dry with materialdried over MgSO4
  5. filtrationAfter filtration and removal of the solvent the residue
  6. customwas chromatographed on silica gel with diethyl ether/hexane 1:3
  7. customsubsequently dried in a high vacuum

出典と根拠

ORDレコード
ord-af29d09869014e7b954582c00483183d
出典データセット
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05990105

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