(S)-tert-Butyl 1-cyclopropyl-3-(2-methoxyethoxy)propan-2-ylcarbamate → (S)-1-Cyclopropyl-3-(2-methoxyethoxy)propan-2-amine

HRID 927596노트

반응식

HRID 927596 반응식
[CH:1]1([CH2:4][C@H:5]([NH:12]C(=O)OC(C)(C)C)[CH2:6][O:7][CH2:8][CH2:9][O:10][CH3:11])[CH2:3][CH2:2]1>Cl.C(OCC)(=O)C.O>[CH:1]1([CH2:4][C@H:5]([NH2:12])[CH2:6][O:7][CH2:8][CH2:9][O:10][CH3:11])[CH2:3][CH2:2]1

참가 물질

4

실험 절차

(S)-tert-Butyl 1-cyclopropyl-3-(2-methoxyethoxy)propan-2-ylcarbamate (1.01 g, 4 mmol) was dissolved in HCl/ethyl acetate (10 mL) and stirred at room temperature for 30 min. Then the reaction mixture was concentrated to give a residue, which was dissolved in H2O (10 mL) and then washed with ethyl acetate (2×10 mL). The pH of the aqueous layer was adjusted to 9˜10 with 5 N NaOH solution. After extraction with ethyl acetate (3×20 mL) the combined organic layers were washed with brine (50 mL), dried over Na2SO4 and concentrated to give the title product (0.072 g, 11%) as yellow oil; MS (EI): m/e=174.2 [M+Na]+.

후처리

  1. concentrationThen the reaction mixture was concentrated
  2. customto give a residue, which
  3. washwashed with ethyl acetate (2×10 mL)
  4. extractionAfter extraction with ethyl acetate (3×20 mL) the combined organic layers
  5. washwere washed with brine (50 mL)
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-28a773d1c58146debffeccff44784b5a
출처 데이터셋
uspto-grants-2016_03
특허 번호
US09290451B2

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