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Sodium Dithionite → 5,6-diamino-1-benzylpyrimidine-2,4(1H,3H)-dione

HRID 2250340
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HRID 2250340 반응식
[NH2:1][C:2]1[N:7]([CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:6](=[O:15])[NH:5][C:4](=[O:16])[C:3]=1[N:17]=O.S(S([O-])=O)([O-])=O.[Na+].[Na+]>N>[NH2:17][C:3]1[C:4](=[O:16])[NH:5][C:6](=[O:15])[N:7]([CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:2]=1[NH2:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24489Sodium DithioniteHCID 33071146-amino-1-benzyl-5-nitrosopyrimidine-2,4(1H,3H)-dione

생성물 1

HCID 107520325,6-diamino-1-benzylpyrimidine-2,4(1H,3H)-dione

시약·촉매·용매 1

HCID 222Ammonia용매

실험 절차

To a solution of 6-amino-5-nitroso-1-benzyl-1,3-dihydropyrimidine-2,4-dione (1.15 g, 4.7 mmol) in 12.5% aqueous ammonia (40 ml) at 70° C. was added sodium hydrosulfite (2.44 g, 14 mmol) in portions over 15 minutes. On cooling the reaction mixture in an ice bath the product precipitated out. It was filtered, washed with water, and dried under reduced pressure, to provide 5,6-diamino-1-benzyl-1,3-dihydropyrimidine-2,4-dione, a compound of formula (21).

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후처리

  1. temperatureOn cooling the reaction mixture in an ice bath the product
  2. customprecipitated out
  3. filtrationIt was filtered
  4. washwashed with water
  5. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-571b0b88be8f408897f5e5c074324a2a
출처 데이터셋
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07317017B2

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