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Acetic Acid → 7,8-Dimethoxyquinazoline-2,4(1H,3H)-dione

HRID 1703365
ノート
印刷プレビュー

反応式

HRID 1703365 の反応式
C(O)(=O)C.[CH3:5][O:6][C:7]1[C:15]([O:16][CH3:17])=[CH:14][CH:13]=[C:9]([C:10]([OH:12])=O)[C:8]=1[NH2:18].[O-:19][C:20]#[N:21].[K+].[OH-].[Na+]>O>[CH3:17][O:16][C:15]1[C:7]([O:6][CH3:5])=[C:8]2[C:9]([C:10](=[O:12])[NH:21][C:20](=[O:19])[NH:18]2)=[CH:13][CH:14]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 176Acetic AcidHCID 14798Sodium HydroxideHCID 11378442Potassium cyanateHCID 117455912-Amino-3,4-dimethoxybenzoic acid

生成物 1

HCID 123200177,8-Dimethoxyquinazoline-2,4(1H,3H)-dione収率 82.3%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
40 °C

実験手順

Acetic acid (177.4 ml., 3.1 moles) was added to a vigorously stirred suspension of 3,4-dimethoxyanthranilic acid (436.5 g., 2.21 moles) in 10 liters of water. Then 2.24 liters of 20% potassium cyanate (5.53 moles) solution was gradually added and the mixture was stirred for one hour at 40° C. After cooling the reaction mixture to 20° C., 3.54 kg. sodium hydroxide pellets were added maintaining the temperature below 40° C. The reaction mixture was heated to 90° C. for 45 minutes and then slowly cooled in an ice bath. The sodium salt of the product was filtered, resuspended in 6 liters of water, acidified with concentrated hydrochloric acid (370 ml.), cooled and filtered to yield 404 grams (82%) of the product. Recrystallization from dimethylformamide gave colorless crystals, M.P. 314°-6° C.

後処理

  1. temperatureAfter cooling the reaction mixture to 20° C.
  2. temperaturemaintaining the temperature below 40° C
  3. temperatureThe reaction mixture was heated to 90° C. for 45 minutes
  4. temperatureslowly cooled in an ice bath
  5. filtrationThe sodium salt of the product was filtered
  6. temperaturecooled
  7. filtrationfiltered

出典と根拠

ORDレコード
ord-14283a8693f34d88bceaafb5800f025c
出典データセット
uspto-grants-1982_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04351940

反応ノート

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