Isoamyl Nitrite → HCID 178508438、化合物

HRID 893607

反応式

HRID 893607 の反応式
[Cl:1][C:2]1[N:7]=[C:6]([NH2:8])[N:5]=[C:4]([NH2:9])[C:3]=1[NH2:10].[N:11](OCCC(C)C)=O>O1CCOCC1>[Cl:1][C:2]1[C:3]2[NH:10][N:11]=[N:9][C:4]=2[N:5]=[C:6]([NH2:8])[N:7]=1

参加物

4

反応物 2

HCID 8053Isoamyl NitriteHCID 5005056-Chloropyrimidine-2,4,5-triamine

生成物 1

HCID 178508438HCID 178508438、化合物収率 78.9%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

A solution of 6-chloro-2,4,5-pyrimidinetriamine (10.94 g, 0.0686 mol) and isoamyl nitrite (9.20 ml, 0.0686 mol)in dioxane (500 ml, freshly purified by passage through basic alumina) was heated under nitrogen with stirring for 2 hours at 90°. The reaction mixture was cooled, treated with activated carbon, filtered, and concentrated to 150 ml. Petroleum ether (250 ml, bp 35-60° ) was added. The precipitate was filtered, washed the petroleum ether (50 ml) and dried in vacuo over P2O5 at 40° for 16 hours to give 9.23 g of crude desired product which was then used in the next step.

後処理

  1. temperaturewas heated under nitrogen
  2. temperatureThe reaction mixture was cooled
  3. additiontreated with activated carbon
  4. filtrationfiltered
  5. concentrationconcentrated to 150 ml
  6. additionPetroleum ether (250 ml, bp 35-60° ) was added
  7. filtrationThe precipitate was filtered
  8. washwashed the petroleum ether (50 ml)
  9. dry with materialdried in vacuo over P2O5 at 40° for 16 hours

出典と根拠

ORDレコード
ord-8a0d8cfa24e945bea6dcdd91058dcd51
出典データセット
uspto-grants-1992_06
特許番号
US05126345

関連ノート

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