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Hydrochloric Acid → 2-(4-Isopropyl-piperazin-1-yl)-pyridin-4-ylamine

HRID 1432147
ノート
印刷プレビュー

反応式

HRID 1432147 の反応式
[CH:1]([N:4]1[CH2:9][CH2:8][N:7]([C:10]2[CH:15]=[C:14]([NH:16]C(=O)C)[CH:13]=[CH:12][N:11]=2)[CH2:6][CH2:5]1)([CH3:3])[CH3:2].Cl>O1CCOCC1>[CH:1]([N:4]1[CH2:5][CH2:6][N:7]([C:10]2[CH:15]=[C:14]([NH2:16])[CH:13]=[CH:12][N:11]=2)[CH2:8][CH2:9]1)([CH3:3])[CH3:2]
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 313Hydrochloric AcidHCID 68946851N-[2-(4-Isopropyl-piperazin-1-yl)-pyridin-4-yl]-acetamide

生成物 1

HCID 617084702-(4-Isopropyl-piperazin-1-yl)-pyridin-4-ylamine収率 57%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

反応条件

温度
100 °C

実験手順

A mixture of 2.1 g (8 mmol) N-[2-(4-isopropyl-piperazin-1-yl)-pyridin-4-yl]-acetamide and 10.5 ml 4N HCl in 25 ml dioxane was heated to 100° C. for 2 h. After evaporation of all volatiles the residue was treated with water and NaHCO3 aq. sat. and extracted with DCM. The combined organic layers were washed with NaCl aq. sat., dried with MgSO4 and evaporated. The residue was triturated with DCM and dried to yield 1 g (57%) of the title compounds as white solid. MS: (m/e): 221.3 (MH+).

後処理

  1. customAfter evaporation of all volatiles the residue
  2. additionwas treated with water and NaHCO3 aq. sat.
  3. extractionextracted with DCM
  4. washThe combined organic layers were washed with NaCl aq. sat.
  5. dry with materialdried with MgSO4
  6. customevaporated
  7. customThe residue was triturated with DCM
  8. customdried

出典と根拠

ORDレコード
ord-47ac73e59fd341cbbfed0b9394cc4976
出典データセット
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07612076B2

反応ノート

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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