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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
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HRID 607140 반응식
[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
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참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-8753127df3b74e789c268af80d8e41d7
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07915411B2

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