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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Cyclopropanecarboximidamide hydrochloride → 2-Cyclopropylpyrimidin-4-ol

HRID 386109
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HRID 386109 반응식
C(O[C:4](=[O:8])/[CH:5]=[CH:6]\[O-])C.[Na+].Cl.[CH:11]1([C:14](=[NH:16])[NH2:15])[CH2:13][CH2:12]1>O>[CH:11]1([C:14]2[N:16]=[C:4]([OH:8])[CH:5]=[CH:6][N:15]=2)[CH2:13][CH2:12]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2781916Cyclopropanecarboximidamide hydrochlorideHCID 58190618sodium (Z)-3-ethoxy-3-oxoprop-1-en-1-olate

생성물 1

HCID 1785164792-Cyclopropylpyrimidin-4-ol

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

Sodium (1Z)-3-ethoxy-3-oxoprop-1-en-1-olate (6.60 g, 47.8 mmol) was dissolved in water (1.5 mL) and in a second flask cyclopropanecarboximidamide hydrochloride (3 g, 24.88 mmol) was dissolved in water (2 mL) and the contents of the second flask were added to the first flask. The reaction was allowed to stir for 72 hours. The reaction was then transferred to a separatory funnel and extracted with chloroform and a small amount of methanol. The water layer was extracted again and the combined organic layers were dried over magnesium sulfate, filtered and concentrated to a pale yellow solid. Diethyl ether was then added to precipitate product. The mixture was filtered and the solid was collected and dried to give the title compound.

후처리

  1. additionthe contents of the second flask were added to the first flask
  2. customThe reaction was then transferred to a separatory funnel
  3. extractionextracted with chloroform
  4. extractionThe water layer was extracted again
  5. dry with materialthe combined organic layers were dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated to a pale yellow solid
  8. additionDiethyl ether was then added
  9. customto precipitate product
  10. filtrationThe mixture was filtered
  11. customthe solid was collected
  12. customdried

출처 및 근거

ORD 기록
ord-708040ad3ea242c584d8d16a9ff0b2e5
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08367706B2

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