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Carbon Dioxide → HCID 14638217, 화합물

HRID 1253180
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HRID 1253180 반응식
Cl[C:2]1[C:7]2[O:8][CH2:9][C:10](=[O:12])[NH:11][C:6]=2[N:5]=[C:4]([CH3:13])[N:3]=1.[CH2:14]([O:16][C:17]([N:19]1[CH2:24][CH2:23][NH:22][CH2:21][CH2:20]1)=[O:18])[CH3:15].C(=O)=O>C(O)CCC>[CH2:14]([O:16][C:17]([N:19]1[CH2:20][CH2:21][N:22]([C:2]2[C:7]3[O:8][CH2:9][C:10](=[O:12])[NH:11][C:6]=3[N:5]=[C:4]([CH3:13])[N:3]=2)[CH2:23][CH2:24]1)=[O:18])[CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 280Carbon DioxideHCID 84311-Piperazinecarboxylic acid, ethyl esterHCID 608089HCID 608089, 화합물

생성물 1

HCID 14638217HCID 14638217, 화합물수율 87%

시약·촉매·용매 1

HCID 2631-Butanol용매

실험 절차

A mixture containing 1 g of 4-chloro-2-methyl-6,7-dihydro-8H-pyrimido[5,4-b][1,4]oxazin-7-one (Khim. Geterotsikl. Soed. 1976, 681), 10 ml of n-butanol and 1.58 g of 1-ethoxycarbonylpiperazine is refluxed under protection against moisture and carbon dioxide, then evaporated. The residue is triturated with water and the product precipitated at 0° to 4° C. is filtered, washed with water and ether and dried to give 1.4 g (87%) of product, m.p.: 197°-198° C.

후처리

  1. customevaporated
  2. customThe residue is triturated with water
  3. customthe product precipitated at 0° to 4° C.
  4. filtrationis filtered
  5. washwashed with water and ether
  6. customdried

출처 및 근거

ORD 기록
ord-5add787aee034512a3e6f1309a0cf981
출처 데이터셋
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04748175

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