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Ethylorthoformate → 9-Benzyl-6-pentyl-6,9-dihydro-5H-[1,2,4]triazolo[3,4-i]purin-5-one

HRID 2374304
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인쇄 미리보기

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HRID 2374304 반응식
[CH2:1]([N:8]1[C:16]2/[C:15](=[N:17]/[NH2:18])/[NH:14][C:13](=[O:19])[N:12]([CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[C:11]=2[N:10]=[CH:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:25]([O-])([O-])OCC>>[CH2:1]([N:8]1[C:16]2[C:15]3=[N:17][N:18]=[CH:25][N:14]3[C:13](=[O:19])[N:12]([CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[C:11]=2[N:10]=[CH:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 53630039EthylorthoformateHCID 178446229HCID 178446229, 화합물

생성물 1

HCID 598538329-Benzyl-6-pentyl-6,9-dihydro-5H-[1,2,4]triazolo[3,4-i]purin-5-one수율 49.5%

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온도
60 °C

실험 절차

(6Z)-7-Benzyl-3-pentyl-3,7-dihydro-1H-purine-2,6-dione 6-hydrazone (0.50 g, 1.5 mmol) was mixed with ethyl orthoformate (5 mL, 30 mmol). After being stirred at 60° C. for 1 h, the reaction mixture was concentrated in vacuum. The residue was treated with ether to yield the desired product as a white solid (0.25 g, 48.5%). LCMS calculated for C18H21N6O (M+H): 337.2; found: 337.1.

후처리

  1. concentrationthe reaction mixture was concentrated in vacuum
  • additionThe residue was treated with ether
  • 출처 및 근거

    ORD 기록
    ord-1f20c25a2c8644a6ad7fbb2bb210a98a
    출처 데이터셋
    uspto-grants-2008_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07462624B2

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