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HCID 3991306, 화합물 → 3-benzyl-5-methyl-1H-pyrimidine-2,4-dione

HRID 342539
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HRID 342539 반응식
C([N:8]1[CH:13]=[C:12]([CH3:14])[C:11](=[O:15])[N:10]([CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:9]1=[O:23])C1C=CC=CC=1>[Pd].C([O-])=O.[NH4+]>[CH2:16]([N:10]1[C:11](=[O:15])[C:12]([CH3:14])=[CH:13][NH:8][C:9]1=[O:23])[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 3991306HCID 3991306, 화합물

생성물 1

HCID 111719463-benzyl-5-methyl-1H-pyrimidine-2,4-dione

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 2723923Ammonium formate용매

실험 절차

A mixture of 1,3-dibenzyl-5-methyl-2,4(1H,3H)-pyrimidinedione (2 g, 6.5 mmol), 5% palladium on carbon (3 g) and 0.4N ammonium formate (250 mL in methanol) was heated 1.5 hours at reflux. The reaction mixture then was filtered and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with methylene chloride/methanol (95:5) to give 3-benzyl-5-methyl-2,4(1H,3H)-pyrimidinedione, m.p. 208°-210° C.

후처리

  1. temperaturewas heated 1.5 hours
  2. temperatureat reflux
  3. filtrationThe reaction mixture then was filtered
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by column chromatography on silica gel eluting with methylene chloride/methanol (95:5)

출처 및 근거

ORD 기록
ord-967537bb05594edb93591d4f289536eb
출처 데이터셋
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05859014

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