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Hydrochloric Acid → 4-Phenyl-1,4,5,6-tetrahydropyrimidin-2-amine hydrochloride

HRID 1296427
ノート
印刷プレビュー

反応式

HRID 1296427 の反応式
[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:5]=[CH:4][N:3]=1.[ClH:14]>C(O)(C)C.[Pd]>[ClH:14].[C:8]1([CH:6]2[NH:7][C:2]([NH2:1])=[N:3][CH2:4][CH2:5]2)[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=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 2

HCID 313Hydrochloric AcidHCID 5987772-Amino-4-phenylpyrimidine

生成物 1

HCID 230261524-Phenyl-1,4,5,6-tetrahydropyrimidin-2-amine hydrochloride収率 55%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 3776Isopropanol溶媒

実験手順

To a solution of 5 g (29.2 mmoles) of 2-amino-4-phenylpyrimidine in 30 ml of a 6N solution of hydrochloric acid in isopropanol was added 0.1 g of palladium on carbon catalyst (10% wt/wt). The suspension was hydrogenated under 40 psi pressure at room temperature during 3 h. The catalyst was removed by filtration and the solvent evaporated under reduced pressure. Diethyl ether was added and the resulting solution was refiltered and the solvent removed by evaporation under reduced pressure to give 4.0 g (55%) of compound as a crude oil which was used as such.

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

後処理

  1. customThe catalyst was removed by filtration
  2. customthe solvent evaporated under reduced pressure
  3. additionDiethyl ether was added
  4. customthe solvent removed by evaporation under reduced pressure

出典と根拠

ORDレコード
ord-5a90afc0f0844978bd4d982e9108f229
出典データセット
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07247638B2

反応ノート

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