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Sulfuric Acid → HCID 19967123、化合物

HRID 2081612
ノート
印刷プレビュー

反応式

HRID 2081612 の反応式
[N:1]1([CH2:6][C:7]2[CH:12]=[CH:11][C:10]([NH:13][C:14](=[O:19])[CH2:15][C:16](=O)[CH3:17])=[CH:9][CH:8]=2)[CH:5]=[CH:4][N:3]=[CH:2]1.S(=O)(=O)(O)O.[OH-].[NH4+]>>[N:1]1([CH2:6][C:7]2[CH:12]=[C:11]3[C:10](=[CH:9][CH:8]=2)[NH:13][C:14](=[O:19])[CH:15]=[C:16]3[CH3:17])[CH:5]=[CH:4][N:3]=[CH:2]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

4

反応物 3

HCID 1118Sulfuric AcidHCID 14923Ammonium HydroxideHCID 19967135HCID 19967135、化合物

生成物 1

HCID 19967123HCID 19967123、化合物収率 34.8%

反応条件

温度
70 °C

実験手順

7 Parts of N-[4-(1H-imidazol-1-ylmethyl)phenyl]-3-oxobutanamide were added dropwise to 73.6 parts of concentrated sulfuric acid (exothermic reaction, the temperature rose to 90° C.). Upon complete addition, the mixture was stirred for 1 hour at 70° C. The reaction mixture was poured into crushed ice and the whole was neutralized with an ammonium hydroxide solution to pH 9. The precipitated product was filtered off and taken up in water. The whole was extracted with dichloromethane. The aqueous layer was concentrated. The crystallized product was filtered off, washed with 2-propanone and dried in vacuo at 100° C., yielding 2.25 parts (34.8%) of 6-(1H-imidazol-1-ylmethyl)-4-methyl-2(1H)-quinolinone; mp. 266.0° C. (compound 1).

後処理

  1. customexothermic reaction
  2. customrose to 90° C.
  3. additionUpon complete addition
  4. additionThe reaction mixture was poured
  5. custominto crushed ice
  6. filtrationThe precipitated product was filtered off
  7. extractionThe whole was extracted with dichloromethane
  8. concentrationThe aqueous layer was concentrated
  9. filtrationThe crystallized product was filtered off
  10. washwashed with 2-propanone
  11. customdried in vacuo at 100° C.

出典と根拠

ORDレコード
ord-5575c2b540234ba7a39bbe867a74b0ec
出典データセット
uspto-grants-1993_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05185346

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート