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Formaldehyde → tert-Butyl 4-[(4-amino-6-methylpyrrolo[2,1-f][1,2,4]triazin-7-yl)methyl]piperazine-1-carboxylate

HRID 1500807
ノート
印刷プレビュー

反応式

HRID 1500807 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]2[N:9]([CH:10]=1)[N:8]=[CH:7][N:6]=[C:5]2[NH2:11].[CH2:12]=O.[N:14]1([C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]1>C(O)(=O)C>[NH2:11][C:5]1[C:4]2=[CH:3][C:2]([CH3:1])=[C:10]([CH2:12][N:17]3[CH2:18][CH2:19][N:14]([C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[CH2:15][CH2:16]3)[N:9]2[N:8]=[CH:7][N:6]=1
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

5

反応物 3

HCID 712FormaldehydeHCID 143452tert-Butyl piperazine-1-carboxylateHCID 552886216-Methylpyrrolo[2,1-f][1,2,4]triazin-4-amine

生成物 1

HCID 86687876tert-Butyl 4-[(4-amino-6-methylpyrrolo[2,1-f][1,2,4]triazin-7-yl)methyl]piperazine-1-carboxylate収率 105%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
60 °C

実験手順

A solution of 6-methylpyrrolo[2,1-f][1,2,4]triazin-4-amine (500 mg, 3.3 mmol; preparation described in PCT Int. Pat. Appl. WO 2007/056170) in acetic acid (8 ml) was treated with 37% aq. formaldehyde solution (328 μl, 4.04 mmol) and tert-butyl piperazine-1-carboxylate (754 mg, 4.04 mmol). The mixture was stirred at 60° C. overnight. After evaporation, the residue was taken up in ethyl acetate and washed with sat. aq. sodium hydrogencarbonate solution. The aqueous layer was extracted twice with ethyl acetate. The combined organic phases were dried over magnesium sulfate and evaporated affording 1.2 g of the crude product which was used in the next step without further purification.

後処理

  1. customAfter evaporation
  2. washwashed with sat. aq. sodium hydrogencarbonate solution
  3. extractionThe aqueous layer was extracted twice with ethyl acetate
  4. dry with materialThe combined organic phases were dried over magnesium sulfate
  5. customevaporated

出典と根拠

ORDレコード
ord-4a30e75a1d6c4eeaafd74b6a7c99a20c
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09206184B2

反応ノート

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