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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hexahydro-1,4-diazepine → 1-pyrimidin-2-yl-1,4-diazepane

HRID 1619215
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HRID 1619215 반응식
[NH:1]1[CH2:7][CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.Cl[C:9]1[N:14]=[CH:13][CH:12]=[CH:11][N:10]=1>C(O)C>[N:10]1[CH:11]=[CH:12][CH:13]=[N:14][C:9]=1[N:1]1[CH2:7][CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1
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참가 물질

4

반응물 2

HCID 68163Hexahydro-1,4-diazepineHCID 744042-Chloropyrimidine

생성물 1

HCID 27724091-pyrimidin-2-yl-1,4-diazepane

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of homopiperazine (3.5 g, 35 mmol) in ethanol (100 ml) at 40° C., was added portionwise 2-chloropyrimidine (2.0 g, 17.5 mmol). The mixture was stirred for 1 hour then concentrated in vacuo. The residue was dissolved in methylene chloride (75 ml) and washed with a saturated solution of sodium bicarbonate and brine. Layers were separated, and the organic layer was dried over magnesium sulfate and concentrated. The resulting residue was purified by flash chromatography and a semi-solid (1.0 g) was collected and used as is.

후처리

  1. concentrationthen concentrated in vacuo
  2. dissolutionThe residue was dissolved in methylene chloride (75 ml)
  3. washwashed with a saturated solution of sodium bicarbonate and brine
  4. customLayers were separated
  5. dry with materialthe organic layer was dried over magnesium sulfate
  6. concentrationconcentrated
  7. customThe resulting residue was purified by flash chromatography
  8. customa semi-solid (1.0 g) was collected

출처 및 근거

ORD 기록
ord-28d31164e63f4d848ec51404d881586d
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772291B2

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