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N-[3-(4-chlorophenyl)-3-(4-fluorophenyl)3-hydroxypropyl]pipecolic acid methyl ester → N-[3-(4-chlorophenyl)-3-(4-fluorophenyl)prop-2-enyl]pipecolic acid methyl ester

HRID 635922
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HRID 635922 반응식
[CH3:1][O:2][C:3](=[O:28])[CH:4]1[CH2:9][CH2:8][CH2:7][CH2:6][N:5]1[CH2:10][CH2:11][C:12]([C:21]1[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][CH:22]=1)([C:14]1[CH:19]=[CH:18][C:17]([F:20])=[CH:16][CH:15]=1)O>C(O)=O>[CH3:1][O:2][C:3](=[O:28])[CH:4]1[CH2:9][CH2:8][CH2:7][CH2:6][N:5]1[CH2:10][CH:11]=[C:12]([C:21]1[CH:22]=[CH:23][C:24]([Cl:27])=[CH:25][CH:26]=1)[C:14]1[CH:19]=[CH:18][C:17]([F:20])=[CH:16][CH:15]=1
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참가 물질

3

반응물 1

HCID 16004955N-[3-(4-chlorophenyl)-3-(4-fluorophenyl)3-hydroxypropyl]pipecolic acid methyl ester

생성물 1

HCID 53685622N-[3-(4-chlorophenyl)-3-(4-fluorophenyl)prop-2-enyl]pipecolic acid methyl ester수율 54%

시약·촉매·용매 1

HCID 284Formic Acid용매

실험 절차

A solution of 0.035 g (0.086 mmol) N-[3-(4-chlorophenyl)-3-(4 fluorophenyl)-3-hydroxypropyl]pipecolic acid methyl ester (Compound B30) in 1 ml 99% formic acid was heated under reflux for 0.5 hours. The mixture was concentrated under vacuum the residue dissolved in ethyl acetate, washed with saturated sodium bicarbonate solution and brine, and the solvent evaporated. The residue was purified by preparative silica gel TLC with 5% diethyl ether in dichlorometane to give 0.018 g (yield 54%) N-[3-(4-chlorophenyl)-3-(4-fluorophenyl)prop-2-enyl]pipecolic acid methyl ester (Compound B20)

후처리

  1. temperatureunder reflux for 0.5 hours
  2. concentrationThe mixture was concentrated under vacuum the residue
  3. dissolutiondissolved in ethyl acetate
  4. washwashed with saturated sodium bicarbonate solution and brine
  5. customthe solvent evaporated
  6. customThe residue was purified by preparative silica gel TLC with 5% diethyl ether in dichlorometane

출처 및 근거

ORD 기록
ord-eb423ea980d045c09c5ce6b60efa76a4
출처 데이터셋
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06191165B1

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