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Sodium ethanethiolate → 5,7-dihydroxy-3-(4-hydroxyphenyl)-4(3H)-quinazolinone

HRID 130333
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HRID 130333 반응식
C[O:2][C:3]1[CH:12]=[C:11]([O:13]C)[CH:10]=[C:9]2[C:4]=1[C:5](=[O:23])[N:6]([C:15]1[CH:20]=[CH:19][C:18]([O:21]C)=[CH:17][CH:16]=1)[CH:7]=[N:8]2.C([S-])C.[Na+]>CN(C=O)C>[OH:2][C:3]1[CH:12]=[C:11]([OH:13])[CH:10]=[C:9]2[C:4]=1[C:5](=[O:23])[N:6]([C:15]1[CH:16]=[CH:17][C:18]([OH:21])=[CH:19][CH:20]=1)[CH:7]=[N:8]2
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참가 물질

4

반응물 2

HCID 4459711Sodium ethanethiolateHCID 116881915,7-Dimethoxy-3-(4-methoxyphenyl)quinazoline-4-one

생성물 1

HCID 104232345,7-dihydroxy-3-(4-hydroxyphenyl)-4(3H)-quinazolinone수율 59%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of 100 mg (0.32 mmol) of 5,7-dimethoxy-3-(4-methoxyphenyl)-4(3H)-quinazolinone as prepared in Example 18 or 19, and 524 mg (6.24 mmol) of sodium ethanethiolate in 2 ml of DMF was refluxed for 3.5 hr. DMF was evaporated and the residue dissolved in water. Concentrated HCl was added to adjust the pH to 5. The precipitate was filtered, dried and purified by chromatography on silica gel (loaded with CH2Cl2 and a slight amount of MeOH, eluted with 70% EtOAc in hexane) to yield 51 mg of 5,7-dihydroxy-3-(4-hydroxyphenyl)-4(3H)-quinazolinone (59%) as an off-white solid.

후처리

  1. temperaturewas refluxed for 3.5 hr
  2. customDMF was evaporated
  3. dissolutionthe residue dissolved in water
  4. additionConcentrated HCl was added
  5. filtrationThe precipitate was filtered
  6. customdried
  7. custompurified by chromatography on silica gel (
  8. washa slight amount of MeOH, eluted with 70% EtOAc in hexane)

출처 및 근거

ORD 기록
ord-9ae930638f1943b7b664b5b0bb346aba
출처 데이터셋
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07381730B2

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