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Methanesulfonyl chloride → methyl (2S,4S)-1-BOC-4-[(4,4-dimethylcyclohexyl)(methylsulfonyl)amino]pyrrolidine-2-carboxylate

HRID 1361309
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HRID 1361309 반응식
[CH3:1][O:2][C:3]([C@@H:5]1[CH2:9][C@H:8]([NH:10][CH:11]2[CH2:16][CH2:15][C:14]([CH3:18])([CH3:17])[CH2:13][CH2:12]2)[CH2:7][N:6]1[C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])=[O:4].[CH3:26][S:27](Cl)(=[O:29])=[O:28]>C(Cl)Cl>[C:19]([N:6]1[CH2:7][C@@H:8]([N:10]([CH:11]2[CH2:16][CH2:15][C:14]([CH3:18])([CH3:17])[CH2:13][CH2:12]2)[S:27]([CH3:26])(=[O:29])=[O:28])[CH2:9][C@H:5]1[C:3]([O:2][CH3:1])=[O:4])([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20]
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4

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HCID 31297Methanesulfonyl chlorideHCID 66970872Methyl(2S,4S)-1-BOC-4-[(4,4-dimethylcyclohexyl)amino]pyrrolidine-2-carboxylate

생성물 1

HCID 66971207methyl (2S,4S)-1-BOC-4-[(4,4-dimethylcyclohexyl)(methylsulfonyl)amino]pyrrolidine-2-carboxylate수율 528.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of methyl (2S,4S)-1-BOC-4-[(4,4-dimethylcyclohexyl)amino]pyrrolidine-2-carboxylate (2.37 g, 6.7 mmol) prepared in Step A of Example A1 in DCM (10 ml) was added TEA (1.36 g, 13.4 mmol), slowly added dropwise methanesulfonylchloride (104 mg, 0.91 mmol) at 0° C., and stirred at rt for 30 min. After the reaction finished, the solvent was concentrated in vacuo, the residue was extracted with water and EtOAc. The organic layer was dried over MgSO4, concentrated in vacuo, and purified by column chromatography (eluent: EtOAc/Hex ═1/1) to give the title compound (2.08 g, 72%).

후처리

  1. concentrationthe solvent was concentrated in vacuo
  2. extractionthe residue was extracted with water and EtOAc
  3. dry with materialThe organic layer was dried over MgSO4
  4. concentrationconcentrated in vacuo
  5. custompurified by column chromatography (eluent: EtOAc/Hex ═1/1)

출처 및 근거

ORD 기록
ord-f60457c97b7a460993f110d5bc9654fe
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07879852B2

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