Bicarbonate Ion → 3-{[3-(2-Chloro-phenyl)-6-fluoro-4-oxo-3,4-dihydro-quinazolin-2-ylmethyl]-amino}-benzonitrile

HRID 1169259노트

반응식

HRID 1169259 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]1[C:17](=[O:18])[C:16]2[C:11](=[CH:12][CH:13]=[C:14]([F:19])[CH:15]=2)[N:10]=[C:9]1[CH:20]=O.[NH2:22][C:23]1[CH:24]=[C:25]([CH:28]=[CH:29][CH:30]=1)[C:26]#[N:27].S([O-])([O-])(=O)=O.[Na+].[Na+].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(=O)(O)[O-]>C(OCC)(=O)C.CCCCCC.C(O)(=O)C>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]1[C:17](=[O:18])[C:16]2[C:11](=[CH:12][CH:13]=[C:14]([F:19])[CH:15]=2)[N:10]=[C:9]1[CH2:20][NH:22][C:23]1[CH:24]=[C:25]([CH:28]=[CH:29][CH:30]=1)[C:26]#[N:27]

참가 물질

8

반응물 5

HCID 769Bicarbonate IonHCID 167023-AminobenzonitrileHCID 24436Sodium SulfateHCID 5049666Sodium triacetoxyborohydrideHCID 106858093-(2-Chlorophenyl)-6-fluoro-3,4-dihydroquinazolin-4-one-2-carboxaldehyde

생성물 1

HCID 102162253-{[3-(2-Chloro-phenyl)-6-fluoro-4-oxo-3,4-dihydro-quinazolin-2-ylmethyl]-amino}-benzonitrile수율 78.2%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 21226206Ethyl acetate hexane용매

실험 절차

A mixture of 3-(2-chloro-phenyl)-6-fluoro-3,4-dihydro-quinazolin-4-one-2-carboxaldehyde (0.150 g, 0.50 mmol), glacial acetic acid (10 mL), 3-aminobenzonitrile (0.050 g, 0.42 mmol), and anhydrous sodium sulfate (0.71 g, 5 mmol) was stirred at ambient temperature overnight. Tlc indicated that the imine had formed (Rf=0.43 on silica gel tic developed with 30% ethyl acetate/hexane, UV detection). Sodium triacetoxyborohydride (0.267 g, 1.26 mmol) was added and the reaction was allowed to stir over the weekend (72 hours). The mixture was poured into saturated aqueous bicarbonate and repeatedly extracted with ethyl acetate. The combined organic layer was dried over magnesium sulfate and concentrated to afford a yellow solid. This solid was triturated with 50% ethyl ether/isopropyl ether to give 0.133 g (78%) of 3-{[3-(2-chloro-phenyl)-6-fluoro-4-oxo-3,4-dihydro-quinazolin-2-ylmethyl]-amino}-benzonitrile as an off white solid which had: mp 225-228° C.; 1H NMR δ 7.93 (dd, J=3, 8 Hz, 1H), 7.87 (dd, J=4.5, 8.5 Hz, 1H), 7.70 (dd, J=1.5, 7.5 Hz, 1H), 7.62-7.52 (m, 4H), 7.40 (dd, J=1.5, 7.5 Hz, 1H), 7.20 (t, J=8 Hz, 1H), 6.97 (d, J=7.5 Hz, 1H), 6.80 (dd, J=2, 8 Hz, 1H), 6.66 (s, 1H), 3.88 (ABq, Δv1-3=39.5 Hz, J=17 Hz, 2H). Analysis calculated for C22H14ClFN4O.0.5 H2O: C, 63.85; H, 3.65; N, 13.54. Found: C, 63.90; H, 3.31; N, 13.46.

후처리

  1. stirringto stir over the weekend (72 hours)
  2. extractionrepeatedly extracted with ethyl acetate
  3. dry with materialThe combined organic layer was dried over magnesium sulfate
  4. concentrationconcentrated
  5. customto afford a yellow solid
  6. customThis solid was triturated with 50% ethyl ether/isopropyl ether

출처 및 근거

ORD 기록
ord-283bb41182194d30ad1bfd49b7ceba8a
출처 데이터셋
uspto-grants-2003_09
특허 번호
US06627755B1

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