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Lithium Hydroxide → Pyrazolo[3,4-d]pyrimidin-4-one

HRID 411585
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HRID 411585 반응식
ClC1C=CC=C(Cl)C=1[N:9]1[C:13]2=[N:14][C:15](CC3C=CC(CC(OCC)=O)=CC=3)=[N:16][C:17](=[O:18])[C:12]2=[C:11](C(C)C)[NH:10]1.C1COCC1.[OH-].[Li+]>O>[N:9]1[C:13]2=[N:14][CH:15]=[N:16][C:17](=[O:18])[C:12]2=[CH:11][N:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3939Lithium HydroxideHCID 8028TetrahydrofuranHCID 178470661HCID 178470661, 화합물

생성물 1

HCID 22252149Pyrazolo[3,4-d]pyrimidin-4-one수율 313.8%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

The ester, 1-(2,6-dichlorophenyl)-3-isopropyl-6-(4-(carbethoxymethyl)benzyl)pyrazolo[3,4-d]pyrimidin-4-one (1.20 g, 2.4 mmol) was stirred at RT overnight with THF (50 mL), water (15 mL) and 1 N lithium hydroxide (7.20 mL). The solution was evaporated to near dryness, diluted with 1 N hydrochloric acid, vigorously stirred and the solid was collected by filtration and dried under high vacuum to give 1-(2,6-dichlorophenyl)-3-isopropyl-6-(4-carboxymethyl)benzyl)pyrazolo[3,4-d]pyrimidin-4-one (1.01 g, 89% yield) as a white solid, mp 212-214° C. Mass Spec.: 471 (M+H)+.

후처리

  1. customThe solution was evaporated
  2. additiondiluted with 1 N hydrochloric acid
  3. filtrationthe solid was collected by filtration
  4. customdried under high vacuum

출처 및 근거

ORD 기록
ord-0fd34822cbd440a0853b57b2b3e44d0e
출처 데이터셋
uspto-grants-2003_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06559152B2

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