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Methanol → 2-(4-((2-Amino-4-methyl-6-(pentylamino)pyrimidin-5-yl)methyl)-3-methoxyphenyl)acetic acid

HRID 2387811
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HRID 2387811 반응식
[OH-:1].[K+].[NH2:3][C:4]1[N:9]=[C:8]([CH3:10])[C:7]([CH2:11][C:12]2[CH:17]=[CH:16][C:15]([CH2:18][C:19]#N)=[CH:14][C:13]=2[O:21][CH3:22])=[C:6]([NH:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[N:5]=1.C[OH:30]>>[NH2:3][C:4]1[N:9]=[C:8]([CH3:10])[C:7]([CH2:11][C:12]2[CH:17]=[CH:16][C:15]([CH2:18][C:19]([OH:30])=[O:1])=[CH:14][C:13]=2[O:21][CH3:22])=[C:6]([NH:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[N:5]=1
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참가 물질

4

반응물 3

HCID 887MethanolHCID 14797Potassium HydroxideHCID 689540842-(4-((2-Amino-4-methyl-6-(pentylamino)pyrimidin-5-yl)methyl)-3-methoxyphenyl)acetonitrile

생성물 1

HCID 689580582-(4-((2-Amino-4-methyl-6-(pentylamino)pyrimidin-5-yl)methyl)-3-methoxyphenyl)acetic acid

반응 조건

온도
65 °C

실험 절차

A 5M aqueous solution of potassium hydroxide (5 mL) was added to a solution of the product from step (vii) (0.60 g) in MeOH (10 mL). The resulting mixture was stirred at 65° C. for 15 h. The mixture was allowed to cool and the solvent evaporated under reduced pressure. The resulting aqueous mixture was neutralised with 2M HCl and extracted with EtOAc. The combined organic phase was dried, filtered and evaporated to give the subtitle compound as a colourless solid 0.329 g that was used without further purification.

후처리

  1. temperatureto cool
  2. customthe solvent evaporated under reduced pressure
  3. extractionextracted with EtOAc
  4. customThe combined organic phase was dried
  5. filtrationfiltered
  6. customevaporated

출처 및 근거

ORD 기록
ord-894a57dcf1204a8cb4eaeabcd05224c5
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08268990B2

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