Pyridine → 3-Benzoylamino-5-nitro-2-pyridone

HRID 66362ノート

反応式

HRID 66362 の反応式
[NH2:1][C:2]1[C:3](=[O:11])[NH:4][CH:5]=[C:6]([N+:8]([O-:10])=[O:9])[CH:7]=1.N1C=CC=CC=1.[C:18](Cl)(=[O:25])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>O>[C:18]([NH:1][C:2]1[C:3](=[O:11])[NH:4][CH:5]=[C:6]([N+:8]([O-:10])=[O:9])[CH:7]=1)(=[O:25])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1

参加物

5

実験手順

A solution of 100 mg. of 3-amino-5-nitro-2-pyridone in 1.5 ml. of pyridine was cooled and treated with 200 mg. of benzoyl chloride. After 2 hours water was added. The oil that separated was washed with water and triturated with ether. The resultant solid was recrystallized from ethyl acetate to give 3-benzoylamino-5-nitro-2-pyridone, m.p. 267°-268° C.

後処理

  1. additiontreated with 200 mg
  2. customThe oil that separated
  3. washwas washed with water
  4. customtriturated with ether
  5. customThe resultant solid was recrystallized from ethyl acetate

出典と根拠

ORDレコード
ord-c14a4005988345be85980af391aebba7
出典データセット
uspto-grants-1978_12
特許番号
US04131677

反応ノート

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