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Glycidol → HCID 14638280, 화합물

HRID 1253185
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HRID 1253185 반응식
[CH2:1]([O:3][C:4]([N:6]1[CH2:11][CH2:10][N:9]([C:12]2[C:17]3[O:18][CH2:19][C:20](=[O:22])[NH:21][C:16]=3[N:15]=[C:14]([CH3:23])[N:13]=2)[CH2:8][CH2:7]1)=[O:5])[CH3:2].[O:24]1[CH2:28][CH:25]1[CH2:26][OH:27]>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.C1C=CC=CC=1>[OH:24][CH:25]([CH2:26][OH:27])[CH2:28][N:21]1[C:20](=[O:22])[CH2:19][O:18][C:17]2[C:12]([N:9]3[CH2:10][CH2:11][N:6]([C:4]([O:3][CH2:1][CH3:2])=[O:5])[CH2:7][CH2:8]3)=[N:13][C:14]([CH3:23])=[N:15][C:16]1=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 11164GlycidolHCID 14638217HCID 14638217, 화합물

생성물 1

HCID 14638280HCID 14638280, 화합물수율 83%

시약·촉매·용매 2

HCID 74236Tetrabutylammonium Bromide촉매HCID 241Benzene용매

실험 절차

A suspension containing 0.96 g of 4-(4-ethoxycarbonyl-1-piperazinyl)-2-methyl-6,7-dihydro-8H-pyrimido[5,4-b][1,4]oxazin-7-one (Example 1), 0.44 g of 2,3-epoxy-1-propanol, 0.0966 g of tetra(n-butyl)-ammonium bromide and 20 ml of abs. benzene is boiled under stirring for 5 hours and left to stand at room temperature overnight. The crystals are filtered, washed with diisopropyl ethyl and dried to give 0.98 g (83%) of the product, m.p.: 146°-148° C.

후처리

  1. waitleft
  2. waitto stand at room temperature overnight
  3. filtrationThe crystals are filtered
  4. washwashed with diisopropyl ethyl
  5. customdried

출처 및 근거

ORD 기록
ord-d74556d18e024ee88bef5af18ecdb376
출처 데이터셋
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04748175

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