(2S,4R)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)-4-fluoropyrrolidine-2-carboxylic acid → (2S,4R)-N-Fmoc-4-fluoropyrrolidine-2-carbonyl fluoride

HRID 220740노트

반응식

HRID 220740 반응식
C(C1C=C(C)C(S(F)(F)[F:13])=C(C)C=1)(C)(C)C.[C:17]([N:34]1[CH2:38][C@H:37]([F:39])[CH2:36][C@H:35]1[C:40](O)=[O:41])([O:19][CH2:20][CH:21]1[C:33]2[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=2)[C:27]2[C:22]1=[CH:23][CH:24]=[CH:25][CH:26]=2)=[O:18]>ClCCl>[C:17]([N:34]1[CH2:38][C@H:37]([F:39])[CH2:36][C@H:35]1[C:40]([F:13])=[O:41])([O:19][CH2:20][CH:21]1[C:33]2[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=2)[C:27]2[C:22]1=[CH:23][CH:24]=[CH:25][CH:26]=2)=[O:18]

참가 물질

4

반응물 2

HCID 10970300(2S,4R)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)-4-fluoropyrrolidine-2-carboxylic acidHCID 441847004-tert-Butyl-2,6-dimethylphenylsulfur trifluoride

생성물 1

HCID 46841192(2S,4R)-N-Fmoc-4-fluoropyrrolidine-2-carbonyl fluoride수율 97%

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

실험 절차

A solution of 4-(tert-butyl)-2,6-dimethylphenylsulfur trifluoride (10.5 mmol) in 5 ml of dichloromethane was added slowly to a stirred solution of (2S,4R)—N-Fmoc-4-fluoropyrrolidine-2-carboxylic acid (7 mmol) in 15 mL of dichloromethane in a fluoropolymer (PFA) reactor cooled on an ice bath. After complete addition, the ice bath was removed and stirred at room temperature for 0.5 h. 19F NMR analysis of the reaction mixture showed that (2S,4R)—N-Fmoc-4-fluoropyrrolidine-2-carbonyl fluoride (Ib) was produced in 97% yield. All the volatiles were removed at reduced pressure, and dichloromethane (2 ml) was added to the residue, followed by the addition of pentane (30 ml). After stirring well, a supernatant liquid was removed and the residue was washed with pentane (25 ml×2). Finally the product (Ib) (1.75 g, 70% yield) was obtained as white powder by dissolving the solid in dichloromethane and precipitating with pentane. 19F-NMR (CDCl3) (a 6:4 mixture of two rotamers) δ 29.69 (s, 0.6 F, COF), 29.39 (s, 0.6 F, COF), −177.05 (m, 0.6 F, CF), −177.99 (m, 0.4 F, CF): 1H-NMR (CDCl3) 8 (as a mixture of rotamers) 2.0-2.9 (m, 2H), 3.4-4.8 (m, 6H), 5.05-5.5 (m, 1H), 7.2-7.9 (m, 8H): 13C-NMR (CDCl3) 8 (as a mixture of two rotamers) δ0.40 (d, J=179.9 Hz, CF), 91.39 (d, J=180.6 Hz, CF), 154.16 (CON), 154.85 (CON), 161.49 (d, J=367.8 Hz, COF): High Resolution Mass/ESI-APCI method (solvent; methanol); (M-F+OCH3+Na)+392.1272 [calcd 392.1269 for (C21H20FNO4+Na)].

후처리

  1. temperaturecooled on an ice bath
  2. additionAfter complete addition
  3. customthe ice bath was removed
  4. customwas produced in 97% yield
  5. customAll the volatiles were removed at reduced pressure, and dichloromethane (2 ml)
  6. additionwas added to the residue
  7. additionfollowed by the addition of pentane (30 ml)
  8. stirringAfter stirring well
  9. customa supernatant liquid was removed
  10. washthe residue was washed with pentane (25 ml×2)
  11. customFinally the product (Ib) (1.75 g, 70% yield) was obtained as white powder
  12. customprecipitating with pentane

출처 및 근거

ORD 기록
ord-c5c15871ab46438fb2cba8c7f5e9fc30
출처 데이터셋
uspto-grants-2012_06
특허 번호
US08203003B2

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