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Bromoacetyl chloride → 6-(Bromoacetyl)-3,4-dihydro-2(1H)-quinazolinone

HRID 979054
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HRID 979054 반응식
[Br:1][CH2:2][C:3](Cl)=[O:4].[NH:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH2:9][NH:8][C:7]1=[O:16].[Cl-].[Al+3].[Cl-].[Cl-]>C(=S)=S>[Br:1][CH2:2][C:3]([C:12]1[CH:11]=[C:10]2[C:15](=[CH:14][CH:13]=1)[NH:6][C:7](=[O:16])[NH:8][CH2:9]2)=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 89602Bromoacetyl chlorideHCID 6451240Aluminum(III) ChlorideHCID 123607561,2,3,4-Tetrahydroquinazolin-2-one

생성물 1

HCID 138271626-(Bromoacetyl)-3,4-dihydro-2(1H)-quinazolinone

시약·촉매·용매 1

HCID 6348Carbon Disulfide용매

실험 절차

Bromoacetyl chloride (6.2 g) is added dropwise to a stirring mixture of 3,4-dihydro-2(1H)-quinazolinone (2.6 g) and anhydrous aluminum chloride (6.3 g) in carbon disulfide (60 ml). The reaction mixture is stirred under reflux for 4.5 hours, the carbon disulfide decanted, and the residue treated with HCl (6N). The resulting solid is poured into ice water, filtered, the filtered solid washed with water and dried in vacuo, affording the desired product, which is used in the next step without further purification.

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후처리

  1. temperatureunder reflux for 4.5 hours
  2. customthe carbon disulfide decanted
  3. additionthe residue treated with HCl (6N)
  4. additionThe resulting solid is poured into ice water
  5. filtrationfiltered
  6. washthe filtered solid washed with water
  7. customdried in vacuo

출처 및 근거

ORD 기록
ord-21cb6f0bea814de4b3d7bfa5f078e69d
출처 데이터셋
uspto-grants-1987_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04666913

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