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Acetic Acid → (R)-tert-Butyl 3-(cyclopropylamino)pyrrolidine-1-carboxylate

HRID 527904
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HRID 527904 반응식
[NH2:1][C@@H:2]1[CH2:6][CH2:5][N:4]([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH2:3]1.C(O[C:17]1(O[Si](C)(C)C)[CH2:19][CH2:18]1)C.C([BH3-])#N.[Na+].C(O)(=O)C>CO>[CH:17]1([NH:1][C@@H:2]2[CH2:6][CH2:5][N:4]([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH2:3]2)[CH2:19][CH2:18]1
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6

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HCID 176Acetic AcidHCID 854070(R)-(+)-1-Boc-3-aminopyrrolidineHCID 2734686(1-Ethoxycyclopropoxy)trimethylsilaneHCID 5003444Sodium cyanoborohydride

생성물 1

HCID 53346626(R)-tert-Butyl 3-(cyclopropylamino)pyrrolidine-1-carboxylate

시약·촉매·용매 1

HCID 887Methanol
용매

실험 절차

To a solution of (R)-tert-butyl 3-aminopyrrolidine-1-carboxylate (400 mg, 2.15 mmol), (1-ethoxycyclopropoxy)trimethylsilane (1500 mg, 8.60 mmol) in methanol (30 mL) was added sodium cyanoborohydride (569 mg, 8.60 mmol) and acetic acid (0.2 mL). The mixture was stirred at reflux for 10 h. The volatiles were removed under reduced pressure. The residue was treated with water (20 mL) and extracted with ethyl acetate (3×30 mL). The combined extracts were washed with brine (3×10 mL), dried over anhydrous Na2SO4, filtered, and concentrated to give the title compound. MS (m/z): 227 (M+H)+.

후처리

  1. temperatureat reflux for 10 h
  2. customThe volatiles were removed under reduced pressure
  3. additionThe residue was treated with water (20 mL)
  4. extractionextracted with ethyl acetate (3×30 mL)
  5. washThe combined extracts were washed with brine (3×10 mL)
  6. dry with materialdried over anhydrous Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-50725f1ae329487eaa7e8374aaab6e08
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09346810B2

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