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Bromine → 7-Bromomethyl-8-propyl-[1,2,4]triazolo[1,5-c]pyrimidine

HRID 898707
ノート
印刷プレビュー

反応式

HRID 898707 の反応式
[Br:1]Br.[CH3:3][C:4]1[N:9]=[CH:8][N:7]2[N:10]=[CH:11][N:12]=[C:6]2[C:5]=1[CH2:13][CH2:14][CH3:15]>CC(O)=O>[Br:1][CH2:3][C:4]1[N:9]=[CH:8][N:7]2[N:10]=[CH:11][N:12]=[C:6]2[C:5]=1[CH2:13][CH2:14][CH3:15]
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 2

HCID 24408BromineHCID 534715537-Methyl-8-propyl-[1,2,4]triazolo[1,5-C]pyrimidine

生成物 1

HCID 575033117-Bromomethyl-8-propyl-[1,2,4]triazolo[1,5-c]pyrimidine

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
100 °C

実験手順

Br2 (0.153 ml, 3 mmol) is added dropwise to a solution of 7-methyl-8-propyl-[1,2,4]triazolo[1,5-c]pyrimidine (3 mmol) heated at 100° C. in HOAc (10 ml). After the addition, the mixture is stirred at 100° C. overnight. The solvent is removed in vacuo and the residue dissolved in EtOAc (15 ml), washed with Na2S2O3 solution (sat. 5 ml), followed by NaHCO3 (10 ml), and brine (10 ml). The organic phase is dried (Na2SO4) and evaporated. The resulting yellow oil is purified by PTLC, which provides the title compound.

後処理

  1. additionAfter the addition
  2. customThe solvent is removed in vacuo
  3. dissolutionthe residue dissolved in EtOAc (15 ml)
  4. washwashed with Na2S2O3 solution (sat. 5 ml)
  5. dry with materialThe organic phase is dried (Na2SO4)
  6. customevaporated
  7. customThe resulting yellow oil is purified by PTLC, which

出典と根拠

ORDレコード
ord-17eaa9ceafd441438d1045638ffd60ea
出典データセット
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07351826B2

反応ノート

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