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Ethyl 5-benzyl-5-azaspiro[2.4]heptane-7-carboxylate → HCID 21978858, 화합물

HRID 729430
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HRID 729430 반응식
C(O[C:4]([CH:6]1[C:10]2([CH2:12][CH2:11]2)[CH2:9][N:8]([CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH2:7]1)=[O:5])C.[CH3:20][Li]>C(OCC)C>[CH2:13]([N:8]1[CH2:7][CH:6]([C:4](=[O:5])[CH3:20])[C:10]2([CH2:11][CH2:12]2)[CH2:9]1)[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1
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4

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HCID 21979521Ethyl 5-benzyl-5-azaspiro[2.4]heptane-7-carboxylateHCID 178418348HCID 178418348, 화합물

생성물 1

HCID 21978858HCID 21978858, 화합물수율 54.6%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

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온도
-10 °C

실험 절차

A solution (−78° C.) of 5-benzyl-5-azaspiro[2.4]heptane-7-carboxylic acid ethyl ester (Example A1a, 8.15 g, 31.4 mmol) in diethyl ether (200 mL) under a nitrogen atmosphere is treated with methyllithium (1.4 M in diethyl ether, 22.4 mL, 31.4 mmol) over a period of 10 minutes. After 1 hour, reaction mixture is warmed to −10° C. and quenched with saturated aqueous ammonium chloride. The mixture is poured into a separatory funnel and the organic layer is washed with saturated aqueous ammonium chloride, water, and brine. The organic layer is then dried with MgSO4, filtered, and the filtrate concentrated. The resulting residue is purified via flash column chromatography (1% triethylamine/7% isopropanol/92% CH2Cl2) to afford the title compound (3.93 g). MS CI: m/z 230 (MH+).

후처리

  1. customreaction mixture
  2. customquenched with saturated aqueous ammonium chloride
  3. additionThe mixture is poured into a separatory funnel
  4. washthe organic layer is washed with saturated aqueous ammonium chloride, water, and brine
  5. dry with materialThe organic layer is then dried with MgSO4
  6. filtrationfiltered
  7. concentrationthe filtrate concentrated
  8. customThe resulting residue is purified via flash column chromatography (1% triethylamine/7% isopropanol/92% CH2Cl2)

출처 및 근거

ORD 기록
ord-3cabc934875349969a6965093f8c1cd7
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07582627B2

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