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Sodium Hydroxide → HCID 59800133, 화합물

HRID 1037578
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HRID 1037578 반응식
[CH3:1][NH:2][C:3]1[N:8]=[C:7]([C:9]2[NH:10][C:11]3[C:16]([CH:17]=2)=[CH:15][C:14]([C:18]([O:20]CC)=[O:19])=[CH:13][CH:12]=3)[CH:6]=[CH:5][N:4]=1.[OH-].[Na+:24]>C(O)C>[Na+:24].[CH3:1][NH:2][C:3]1[N:8]=[C:7]([C:9]2[NH:10][C:11]3[C:16]([CH:17]=2)=[CH:15][C:14]([C:18]([O-:20])=[O:19])=[CH:13][CH:12]=3)[CH:6]=[CH:5][N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 59800135Ethyl 2-[2-(methylamino)pyrimidin-4-yl]-1H-indole-5-carboxylate

생성물 1

HCID 59800133HCID 59800133, 화합물수율 100%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

25 g of ethyl 2-(2-methylaminopyrimidin-4-yl)-1H-indole-5-carboxylate were admixed with 200 ml of ethanol and 24.5 g of 33% sodium hydroxide solution, and heated to from 65° C. to 70° C. for 4 h. After cooling, the mixture was filtered with suction and the precipitate was washed with 15 ml of ethanol/water (9:1). 24.5 g (87.6% of theory) of 2-(2-methylaminopyrimidin-4-yl)-1H-indole-5-carboxylic acid sodium salt were obtained (98.1 HPLC area %). LCMS: [M+H]⊕ 269.10

후처리

  1. temperatureheated to from 65° C. to 70° C. for 4 h
  2. temperatureAfter cooling
  3. filtrationthe mixture was filtered with suction
  4. washthe precipitate was washed with 15 ml of ethanol/water (9:1)

출처 및 근거

ORD 기록
ord-fc540dc49b2b432db08a248bf1c48d95
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08546567B2

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