Tetrahydrofuran → 2-[7-(3-Fluoro-benzyloxy)-2-methyl-4-oxo-4H-quinazolin-3-yl]-acetamide

HRID 7629

반응식

HRID 7629 반응식
[F:1][C:2]1[CH:3]=[C:4]([CH:19]=[CH:20][CH:21]=1)[CH2:5][O:6][C:7]1[CH:15]=[CH:14][C:10]([C:11]([OH:13])=O)=[C:9]([N+:16]([O-])=O)[CH:8]=1.FC1C=C(C=CC=1)COC(=O)[C:29]1C=CC(OCC2C=CC=C(F)C=2)=C[C:30]=1[N+:44]([O-])=O.COC(=O)C1C=CC(OCC2C=CC=C(F)C=2)=CC=1[N+:69]([O-])=O.O.[OH-].[Li+].[OH-].[Na+].[CH2:78]1[CH2:82][O:81]CC1>O>[F:1][C:2]1[CH:3]=[C:4]([CH:19]=[CH:20][CH:21]=1)[CH2:5][O:6][C:7]1[CH:8]=[C:9]2[C:10]([C:11](=[O:13])[N:44]([CH2:78][C:82]([NH2:69])=[O:81])[C:30]([CH3:29])=[N:16]2)=[CH:14][CH:15]=1

참가 물질

8

실험 절차

4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid: A mixture of 4-(3-fluorobenzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) ester and 4-(3-fluoro-benzyloxy)-2-nitro-benzoic acid methyl ester (14.0 g, 35.0 mmol) in THF (120 mL) and water (120 mL), containing lithium hydroxide monohydrate (2.94 g, 70.1 mmol) was stirred at rt for 48 h. Then the mixture was poured into sodium hydroxide (2 N, 50 mL) and then the mixture extracted with diethyl ether (3×150 mL). The aqueous phase was then adjusted to pH 2 with HCl. Then the mixture was poured into sodium hydroxide (2 N, 50 mL) and the aqueous phase was then adjusted to pH 5.2 with HCl then the mixture extracted with diethyl ether (3×100 mL). The combined extracts were then washed with brine (100 mL) dried and evaporated to afford title compound (6.6 g, 65%) as a light yellow solid. MS: m/e=290.0 (M−H).

후처리

  1. extractionthe mixture extracted with diethyl ether (3×150 mL)
  2. additionThen the mixture was poured into sodium hydroxide (2 N, 50 mL)
  3. extractionthe mixture extracted with diethyl ether (3×100 mL)
  4. washThe combined extracts were then washed with brine (100 mL)
  5. customdried
  6. customevaporated

출처 및 근거

ORD 기록
ord-ad3689421b0444ecba177dceb56a6917
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07087612B2

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