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Isopropanol → Amdoxovir

HRID 227462
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인쇄 미리보기

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HRID 227462 반응식
C([O:6][CH2:7][C@H:8]1[O:12][C@@H:11]([N:13]2[CH:21]=[N:20][C:19]3[C:14]2=[N:15][C:16]([NH2:23])=[N:17][C:18]=3[NH2:22])[CH2:10][O:9]1)(=O)C(C)C.CC(O)C>N>[NH2:23][C:16]1[N:15]=[C:14]2[C:19]([N:20]=[CH:21][N:13]2[C@H:11]2[CH2:10][O:9][C@@H:8]([CH2:7][OH:6])[O:12]2)=[C:18]([NH2:22])[N:17]=1
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참가 물질

4

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HCID 3776IsopropanolHCID 16050140(2R,4R)-2-isobutyryloxymethyl-4-(2,6-diaminopurin-9-yl)-1,3-dioxolane

생성물 1

HCID 124088Amdoxovir수율 83%

시약·촉매·용매 1

HCID 222Ammonia용매

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온도
25 °C

실험 절차

31.05 g of (2R,4R)-2-isobutyryloxymethyl-4-(2,6-diaminopurin-9-yl)-1,3-dioxolane×2-propanol (cf. Example 4) were dissolved in 310 ml of NH3-saturated methanol. The solution was stirred at 25° C. for 15 h, and the solvent was distilled off in vacuo. The residue was recrystallized from ethanol/water. 17.10 g (83%) of (−)-DAPD were obtained as colorless crystals.

후처리

  1. distillationthe solvent was distilled off in vacuo
  2. customThe residue was recrystallized from ethanol/water

출처 및 근거

ORD 기록
ord-b8b1fe9c93ec488987e4594a347b4e5b
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07560550B2

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