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Water → 3-(3-Chloro-5-fluorophenyl)-1-ethylazetidin-3-ol

HRID 2041887
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HRID 2041887 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2([OH:13])[CH2:12][NH:11][CH2:10]2)[CH:5]=[C:6]([F:8])[CH:7]=1.C(=O)([O-])[O-].[K+].[K+].I[CH2:21][CH3:22].O>C(#N)C.C(OCC)(=O)C>[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2([OH:13])[CH2:12][N:11]([CH2:21][CH3:22])[CH2:10]2)[CH:5]=[C:6]([F:8])[CH:7]=1
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참가 물질

7

반응물 4

HCID 962WaterHCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 669953933-(3-Chloro-5-fluorophenyl)azetidin-3-ol

생성물 1

HCID 462081073-(3-Chloro-5-fluorophenyl)-1-ethylazetidin-3-ol수율 60.1%

시약·촉매·용매 2

HCID 6342Acetonitrile용매
HCID 8857
Ethyl Acetate
용매

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온도
120 °C

실험 절차

A mixture of 3-(3-chloro-5-fluorophenyl)azetidin-3-ol (0.41 g, 2.03 mmol), potassium carbonate (0.56 g, 4.06 mmol) and iodoethane (0.31 g, 2.03 mmol) in acetonitrile (5 ml) was heated at 120° C. under microwave irradiation for 10 min. Water (50 ml) and ethyl acetate (50 ml) was added and the organic phase was collected. The aqueous phase was extracted with ethyl acetate (2×50 ml). The combined organic phase was dried (Na2SO4) and evaporated under reduced pressure to give the crude product. Purification by flash column chromatography on silica gel (ethyl acetate) gave 0.28 g (60%) of the title compound. The amine was converted to the fumaric acid salt and recrystallized from ethanol/diethyl ether/diisopropyl ether: M.p. 166-168° C. MS m/z (relative intensity, 70 eV) 229 (M+, 1), 172 (23), 130 (24), 109 (33), 58 (bp).

후처리

  1. customthe organic phase was collected
  2. extractionThe aqueous phase was extracted with ethyl acetate (2×50 ml)
  3. dry with materialThe combined organic phase was dried (Na2SO4)
  4. customevaporated under reduced pressure
  5. customto give the crude product
  6. customPurification by flash column chromatography on silica gel (ethyl acetate)

출처 및 근거

ORD 기록
ord-4652aae95b8240f3b3f5d251a489b02e
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08586572B2

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