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Hydrochloride methanol → HCID 67582048, 화합물

HRID 1416494
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HRID 1416494 반응식
[OH:1][C@@H:2]([C@H:21]([OH:23])[CH3:22])[CH2:3][O:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[N:8]=[C:7]([N:15]2[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]2)[N:6]=1.[ClH:24].CO>CO>[ClH:24].[OH:1][C@@H:2]([C@H:21]([OH:23])[CH3:22])[CH2:3][O:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[N:8]=[C:7]([N:15]2[CH2:16][CH2:17][NH:18][CH2:19][CH2:20]2)[N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21893726Hydrochloride methanolHCID 54302337HCID 54302337, 화합물

생성물 1

HCID 67582048HCID 67582048, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

4-[(2R,3R)-(2,3-Dihydroxybutan-1-yl)oxy]-2-(1-piperazinyl)quinazoline (cf. Example 55) (0.85 g) is dissolved in methanol (10 ml), and thereto is added 2N HCl-methanol (1.6 ml), and the mixture is evaporated to dryness under reduced pressure. The resulting residue is recrystallized from ethanol to give 4-[(2R,3R)-(2,3-dihydroxybutan-1-yl)oxy]-2-(1-piperazinyl)quinazoline monohydrochloride (0.3 g).

후처리

  1. custom
the mixture is evaporated to dryness under reduced pressure
  • customThe resulting residue is recrystallized from ethanol
  • 출처 및 근거

    ORD 기록
    ord-7b3bbd62f6174f178d64a52c98e44f8a
    출처 데이터셋
    uspto-grants-1999_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05912247

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