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Nitric Acid → 5,6-Dichloro-3-nitropyrazin-2-amine

HRID 1648848
ノート
印刷プレビュー

反応式

HRID 1648848 の反応式
S(=O)(=O)(O)O.[NH2:6][C:7]1[C:8](C(O)=O)=[N:9][C:10]([Cl:14])=[C:11]([Cl:13])[N:12]=1.[N+:18]([O-])([OH:20])=[O:19]>>[Cl:14][C:10]1[N:9]=[C:8]([N+:18]([O-:20])=[O:19])[C:7]([NH2:6])=[N:12][C:11]=1[Cl:13]
参加物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 944Nitric AcidHCID 1118Sulfuric Acid2 回HCID 3432713-Amino-5,6-dichloropyrazine-2-carboxylic acid

生成物 1

HCID 130629765,6-Dichloro-3-nitropyrazin-2-amine

実験手順

To 450 ml concentrated sulfuric acid cooled to 10° is added 50.0 g (0.2 m) 3-amino-5,6-dichloropyrazine carboxylic acid. To this solution cooled to 0°-5°, is added a cold solution of 15 ml fuming sulfuric acid in 15 ml fuming nitric acid dropwise over 15 minutes. The reaction mixture is stirred at 0°-5° for 2 hours and then at ambient temperature for 2 hours. The reaction mixture is then poured onto ice and the yellow solid is collected. This solid is taken up in ethyl acetate, washed twice with saturated sodium carbonate solution and then the solution is filtered through a pad of silica gel. The resulting solution is evaporated in vacuo to afford 35 g of 5,6-dichloro-3-nitropyrazinamine, m.p. 169°-170° C.

後処理

  1. temperatureTo this solution cooled to 0°-5°
  2. additionis added a cold solution of 15 ml
  3. customdropwise over 15 minutes
  4. waitat ambient temperature for 2 hours
  5. additionThe reaction mixture is then poured onto ice
  6. customthe yellow solid is collected
  7. washwashed twice with saturated sodium carbonate solution
  8. filtrationthe solution is filtered through a pad of silica gel
  9. customThe resulting solution is evaporated in vacuo

出典と根拠

ORDレコード
ord-18219f3f825e4510a64e1d37561fe59d
出典データセット
uspto-grants-1983_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04414215

反応ノート

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