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Formamidine acetate → 4(1H)-Quinazolinone

HRID 454016
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HRID 454016 반응식
[NH2:1][C:2]1[C:7]([C:8]([O:10]CC)=O)=[CH:6][C:5](OC)=[C:4](OCC2CCN(C)CC2)[CH:3]=1.C(O)(=O)C.[CH:28](N)=[NH:29]>COCCO>[N:1]1[C:2]2[C:7](=[CH:6][CH:5]=[CH:4][CH:3]=2)[C:8](=[O:10])[NH:29][CH:28]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 160693Formamidine acetate2회HCID 21874813Ethyl 2-amino-5-methoxy-4-((1-methylpiperidin-4-yl)methoxy)benzoate

생성물 1

HCID 1354087534(1H)-Quinazolinone수율 173.8%

시약·촉매·용매 1

HCID 80192-Methoxyethanol용매

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온도
115 °C

실험 절차

A solution of ethyl 6-amino-3-methoxy-4-(1-methylpiperidin-4-ylmethoxy)benzoate (16.1 g, 50 mmol) in 2-methoxyethanol (160 ml) containing formamidine acetate (5.2 g, 50 mmol) was heated at 115° C. for 2 hours. Formamidine acetate (10.4 g, 100 mmol) was added in portions every 30 minutes during 4 hours. Heating was prolonged for 30 minutes after the last addition. After cooling, the volatiles were removed under vacuum. The solid was dissolved in ethanol (100 ml) and methylene chloride (50 ml). The precipitate was removed by filtration and the filtrate was concentrated to a final volume of 100 ml. The suspension was cooled to 5° C. and the solid was collected by filtration, washed with cold ethanol followed by ether and dried under vacuum overnight at 60° C. to give 6-methoxy-74(1-methylpiperidin-4-yl)methoxy)-3,4-dihydroquinazolin-4-one (12.7 g, 70%).

후처리

  1. temperatureHeating
  2. additionafter the last addition
  3. temperatureAfter cooling
  4. customthe volatiles were removed under vacuum
  5. dissolutionThe solid was dissolved in ethanol (100 ml)
  6. customThe precipitate was removed by filtration
  7. concentrationthe filtrate was concentrated to a final volume of 100 ml
  8. temperatureThe suspension was cooled to 5° C.
  9. filtrationthe solid was collected by filtration
  10. washwashed with cold ethanol
  11. customdried under vacuum overnight at 60° C.

출처 및 근거

ORD 기록
ord-2d51471139874b3a844b51adb6d211f9
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08492560B2

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