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Hydrochloric Acid → 6,7-Dimethoxy-2,4(1H,3H)-quinazolinedione

HRID 579731
ノート
印刷プレビュー

反応式

HRID 579731 の反応式
[NH2:1][C:2]1[CH:10]=[C:9]([O:11][CH3:12])[C:8]([O:13][CH3:14])=[CH:7][C:3]=1[C:4]([OH:6])=O.Cl.[C-:16]#[N:17].[K+].[OH-:19].[Na+].S(=O)(=O)(O)O>O1CCCC1.O>[CH3:14][O:13][C:8]1[CH:7]=[C:3]2[C:2](=[CH:10][C:9]=1[O:11][CH3:12])[NH:1][C:16](=[O:19])[NH:17][C:4]2=[O:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 313Hydrochloric AcidHCID 1118Sulfuric AcidHCID 9032Potassium CyanideHCID 14798Sodium HydroxideHCID 797364,5-Dimethoxyanthranilic acid

生成物 1

HCID 1200816,7-Dimethoxy-2,4(1H,3H)-quinazolinedione収率 54.9%

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
2 回
HCID 8028Tetrahydrofuran溶媒

実験手順

21 g of 2-Amino-4,5-dimethoxy benzoic acid was dissolved in 40 ml of tetrahydrofuran and 40 ml of water. To this solution 10 ml of conc. hydrochloric acid and 11.6 g of potassium cyanide were added. It was left to stand overnight and 50 g of sodium hydroxide was added. After stirring for 2 hours, the resulting precipitate was isolated by filtration. The precipitate was dissolved in 1000 ml of water and acidified with 50% sulfuric acid. The resulting crystal was isolated by filtration and 13.0 g of the desired compound was obtained. m.p. 320° C. (decomp).

後処理

  1. waitIt was left
  2. customthe resulting precipitate was isolated by filtration
  3. customThe resulting crystal was isolated by filtration

出典と根拠

ORDレコード
ord-76d5bbb2a31649f3aea0d966c00686c5
出典データセット
uspto-grants-1988_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04749705

反応ノート

読み込み中…

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