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Potassium Hydroxide → 2,4-Bis[[(2,3-difluorophenyl)methyl]thio]-7-pteridinamine

HRID 1789937
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HRID 1789937 반응식
[NH2:1][C:2]1[C:7]([NH:8][CH2:9][C:10]#[N:11])=[C:6]([S:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([F:20])[C:15]=2[F:21])[N:5]=[C:4]([S:22][CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[C:26]([F:30])[C:25]=2[F:31])[N:3]=1.[OH-].[K+]>CO.ClCCl>[F:31][C:25]1[C:26]([F:30])=[CH:27][CH:28]=[CH:29][C:24]=1[CH2:23][S:22][C:4]1[N:5]=[C:6]([S:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([F:20])[C:15]=2[F:21])[C:7]2[C:2](=[N:1][C:10]([NH2:11])=[CH:9][N:8]=2)[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14797Potassium HydroxideHCID 22037045[[4-Amino-2,6-bis[[(2,3-difluorophenyl)methyl]thio]-5-pyrimidinyl]amino]acetonitrile

생성물 1

HCID 220370392,4-Bis[[(2,3-difluorophenyl)methyl]thio]-7-pteridinamine

시약·촉매·용매 2

HCID 887Methanol용매HCID 6344Dichloromethane용매

실험 절차

A solution of the product from example 1 step b) (1.35 g) and potassium hydroxide (114 mg) in methanol (50 ml) and dichloromethane (20 ml) was stirred at room temperature for 24 hours. After evaporation in vacuo, the residue was purified by silica gel flash column chromatography, eluting with 5:1 dichloromethane:ethyl acetate, to give the subtitled compound as a pale yellow solid (0.37 g).

후처리

  1. customAfter evaporation in vacuo
  2. customthe residue was purified by silica gel flash column chromatography
  3. washeluting with 5:1 dichloromethane

출처 및 근거

ORD 기록
ord-5fd2ccf2dc594170826f4d7c291c7658
출처 데이터셋
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07071193B2

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