Anthranilic Acid → 2-(4-Oxo-3,4-dihydroquinazolin-2-yl)acetonitrile

HRID 2283197ノート

反応式

HRID 2283197 の反応式
[C:1]([CH2:3][C:4](=S)[NH2:5])#[N:2].BrCC.[O-]CC.[Na+].[NH2:14][C:15]1[CH:23]=[CH:22][CH:21]=[CH:20][C:16]=1[C:17]([OH:19])=O>>[O:19]=[C:17]1[C:16]2[C:15](=[CH:23][CH:22]=[CH:21][CH:20]=2)[N:14]=[C:4]([CH2:3][C:1]#[N:2])[NH:5]1

参加物

5

反応物 4

HCID 227Anthranilic AcidHCID 6332Ethyl BromideHCID 14162772-CyanoethanethioamideHCID 2723922Sodium ethoxide

生成物 1

HCID 1354090772-(4-Oxo-3,4-dihydroquinazolin-2-yl)acetonitrile収率 47.1%

実験手順

2-Cyanoethanethioamide (1.00 g, 10.0 mmol) and bromoethane (821 μL, 11.0 mmol) were added to an ethanolic solution of sodium ethoxide (11.5 mmol, 5.3 mL). The resulting mixture was stirred for 6 hours, 2-aminobenzoic acid (1.50 g, 10.9 mmol) was added, and the reaction was refluxed overnight with stirring. A solid precipitate formed upon cooling of the reaction mixture, which was recovered by vacuum filtration and washed sequentially with ethanol, water, ethanol, and diethyl ether. The solid was then dried to yield 2-(4-oxo-3,4-dihydroquinazolin-2-yl)acetonitrile (872 mg, 47%). 1NMR (400 MHz, DMSO-d6) δ ppm 4.17 (s, 2H), 7.53 (t, J=7.5 Hz, 1H), 7.68 (d, J=7.9 Hz, 1H), 7.83 (t, J=7.8 Hz, 1H), 8.10 (dd, J1=7.9 Hz, J2=1.2 Hz, 1H).

後処理

  1. temperaturethe reaction was refluxed overnight
  2. stirringwith stirring
  3. customA solid precipitate formed
  4. temperatureupon cooling of the reaction mixture, which
  5. filtrationwas recovered by vacuum filtration
  6. washwashed sequentially with ethanol, water, ethanol, and diethyl ether
  7. customThe solid was then dried

出典と根拠

ORDレコード
ord-87dd7746e3de4960a9932acef889498b
出典データセット
uspto-grants-2015_09
特許番号
US09145376B2

反応ノート

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