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Sodium Hydroxide → 1-(2-Phenyl-4-quinazolinyl)-4-piperidinol

HRID 1659950
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HRID 1659950 반응식
[C:1]1([C:7]2[N:16]=[C:15](Cl)[C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH:18][CH:19]1[CH2:24][CH2:23][NH:22][CH2:21][CH2:20]1.[OH-].[Na+]>C(O)C>[C:1]1([C:7]2[N:16]=[C:15]([N:22]3[CH2:23][CH2:24][CH:19]([OH:18])[CH2:20][CH2:21]3)[C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 79341Piperidin-4-olHCID 809774-Chloro-2-phenylquinazoline

생성물 1

HCID 127960301-(2-Phenyl-4-quinazolinyl)-4-piperidinol수율 41.9%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture containing 6 g (0.025 mole) of 2-phenyl-4-chloroquinazoline, 3,53 g (0.035 mole) of 4-hydroxypiperidine and 100 ml of 95% ethyl alcohol was refluxed for 3 hrs. One gram of sodium hydroxide (in one ml of water) was added and the mixture was refluxed for an additional 2 hr period. The mixture was filtered and the filtrate was added to 300 ml of water. The white crystalline precipitate was separated and recrystallized with methanol and water to give 3.2 g of the title compound, m.p. 165°-167° C.

후처리

  1. temperaturewas refluxed for 3 hrs
  2. temperaturethe mixture was refluxed for an additional 2 hr period
  3. filtrationThe mixture was filtered
  4. additionthe filtrate was added to 300 ml of water
  5. customThe white crystalline precipitate was separated
  6. customrecrystallized with methanol and water

출처 및 근거

ORD 기록
ord-a273db0bd9e443a991e634c945e96112
출처 데이터셋
uspto-grants-1981_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04306065

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