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2,2-Dimethyl-1,3-dioxane-4,6-dione → 2,2-Dimethyl-5-[(2-propyl-thiazol-5-ylamino)-methylene]-[1,3]dioxane-4,6-dione

HRID 607140
ノート
印刷プレビュー

反応式

HRID 607140 の反応式
[CH2:1]([C:4]1[S:5][C:6]([NH2:9])=[CH:7][N:8]=1)[CH2:2][CH3:3].[CH3:10][C:11]1([CH3:19])[O:18][C:16](=[O:17])[CH2:15][C:13](=[O:14])[O:12]1.[CH2:20](OC(OCC)OCC)C>C(O)C>[CH3:10][C:11]1([CH3:19])[O:18][C:16](=[O:17])[C:15](=[CH:20][NH:9][C:6]2[S:5][C:4]([CH2:1][CH2:2][CH3:3])=[N:8][CH:7]=2)[C:13](=[O:14])[O:12]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 3

HCID 162492,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 31214Ethyl orthoformateHCID 451217592-Propylthiazol-5-amine

生成物 1

HCID 668083152,2-Dimethyl-5-[(2-propyl-thiazol-5-ylamino)-methylene]-[1,3]dioxane-4,6-dione収率 54.1%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A solution of the product of Example 5D (212.7 mg, 1.496 mmol) in anhydrous ethanol (5 mL) was treated with Meldrum's acid (237 mg, 1.645 mmol) and triethylorthoformate (0.25 mL, 1.496 mmol) at room temperature, and the reaction was heated in a preheated 100° oil bath. After 15 minutes, the reaction was cooled to room temperature and the solvent removed by rotary evaporation under vacuum. Purification by silica gel flash chromatography with a gradient of 10% to 20% ethyl acetate/methylene chloride afforded the title compound as an off-white solid (240 mg, 0.8099 mmol, 54%).

後処理

  1. temperaturethe reaction was heated in a preheated 100° oil bath
  2. customthe solvent removed by rotary evaporation under vacuum
  3. customPurification by silica gel flash chromatography with a gradient of 10% to 20% ethyl acetate/methylene chloride

出典と根拠

ORDレコード
ord-8753127df3b74e789c268af80d8e41d7
出典データセット
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07915411B2

反応ノート

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