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Acetone → HCID 67581958, 화합물

HRID 1416462
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HRID 1416462 반응식
[OH:1][C@H:2]1[C@@H:6]([OH:7])[C@H](OC)[CH2:4][C@@H:3]1[O:10][C:11]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[N:14]=[C:13]([N:21]2[CH2:26][CH2:25][NH:24][CH2:23][CH2:22]2)[N:12]=1.[ClH:27].CO.CC(C)=O>CO>[ClH:27].[OH:1][C@@H:2]1[CH2:6][O:7][CH2:4][C@H:3]1[O:10][C:11]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[N:14]=[C:13]([N:21]2[CH2:22][CH2:23][NH:24][CH2:25][CH2:26]2)[N:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 180AcetoneHCID 21893726Hydrochloride methanolHCID 57098847HCID 57098847, 화합물

생성물 1

HCID 67581958HCID 67581958, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

4-[(3R,4R)-(4-Hydroxytetrahydrofuran-3-yl)oxy]-2-(1-piperazinyl)quinazoline 1/2 hydrochloride (cf. Example 21) (178 mg) is dissolved in methanol (3 ml) with heating, and thereto is added 2N HCl-methanol (0.32 ml) and acetone (10 ml), and the mixture is allowed to stand at room temperature. The precipitated crystals are separated by filtration to give 4-[(3R,4R)-(4-hydroxytetrahydrofuran-3-yl)oxy]-2-(1-piperazinyl)quinazoline monohydrochloride (124 mg) as crystals.

후처리

  1. temperaturewith heating
  2. customto stand at room temperature
  3. customThe precipitated crystals are separated by filtration

출처 및 근거

ORD 기록
ord-6367e3b9599b47dbbc79ba559e682083
출처 데이터셋
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05912247

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