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6-Amino-3-butyl-1,3-dihydropyrimidine-2,4-dione → 5-Nitroso-6-amino-3-butyl-1,3-dihydropyrimidine-2,4-dione

HRID 2213845
ノート
印刷プレビュー

反応式

HRID 2213845 の反応式
[NH2:1][C:2]1[NH:7][C:6](=[O:8])[N:5]([CH2:9][CH2:10][CH2:11][CH3:12])[C:4](=[O:13])[CH:3]=1.[N:14]([O-])=[O:15].[Na+]>C(O)(=O)C>[N:14]([C:3]1[C:4](=[O:13])[N:5]([CH2:9][CH2:10][CH2:11][CH3:12])[C:6](=[O:8])[NH:7][C:2]=1[NH2:1])=[O:15]
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 2

HCID 139476326-Amino-3-butyl-1,3-dihydropyrimidine-2,4-dioneHCID 23668193Sodium Nitrite

生成物 1

HCID 149697085-Nitroso-6-amino-3-butyl-1,3-dihydropyrimidine-2,4-dione

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
70 °C

実験手順

A mixture of 6-amino-3-butyl-1,3-dihydropyrimidine-2,4-dione (4.0 g, 21.88 mmol) and aqueous acetic acid (120 ml) was heated at 70° C. until complete solution as attained, and the solution was cooled to 30° C. Sodium nitrite (3 g) was added in small portions while stirring, forming an orange precipitate. The reaction mixture was cooled to 0° C., and the precipitate filtered off, washed with water, and dried under reduced pressure, to provide 5-nitroso-6-amino-3-butyl-1,3-dihydropyrimidine-2,4-dione, which was used in the next reaction with no further purification.

後処理

  1. temperaturethe solution was cooled to 30° C
  2. customforming an orange precipitate
  3. temperatureThe reaction mixture was cooled to 0° C.
  4. filtrationthe precipitate filtered off
  5. washwashed with water
  6. customdried under reduced pressure

出典と根拠

ORDレコード
ord-f03cf83f8bf040a09c64c8dda943cac0
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07105665B2

反応ノート

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