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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 2250338
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HRID 2250338 반응식
[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]
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참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
70 °C

실험 절차

A mixture of 6-amino-3-butyl-1,3-dihydropyrimidine-2,4-dione (4.0 g, 21.8 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.

후처리

  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

출처 및 근거

ORD 기록
ord-24c5306defee41af881ae78a5b72bc3d
출처 데이터셋
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07317017B2

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