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Dimethyl Sulfoxide → Benzyl 2-methyl-5-oxopiperidine-1-carboxylate

HRID 1852751
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HRID 1852751 반응식
C(Cl)(=O)C(Cl)=O.CS(C)=O.[OH:11][C@@H:12]1[CH2:17][N:16]([C:18]([O:20][CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)=[O:19])[C@@H:15]([CH3:28])[CH2:14][CH2:13]1.C(N(CC)CC)C>C(Cl)Cl>[CH3:28][CH:15]1[CH2:14][CH2:13][C:12](=[O:11])[CH2:17][N:16]1[C:18]([O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 86724498benzyl (2S,5S)-5-hydroxy-2-methylpiperidine-1-carboxylate

생성물 1

HCID 71305938Benzyl 2-methyl-5-oxopiperidine-1-carboxylate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of oxalyl chloride (13.17 mL, 0.150 mol) in CH2Cl2 (250 mL) at −78° C. was added DMSO (14.23 mL, 0.201 mol) dropwise. The reaction was aged for 20 min at −78° C., then ±Benzyl trans-5-hydroxy-2-methylpiperidine-1-carboxylate (25.0 g, 0.100 mol) was added dropwise over 10 min and aged for an additional 10 min before triethylamine (41.9 mL, 0.301 mol) was added dropwise over 5 min at −78° C. The reaction was warmed to room temperature, then quenched with addition of half-saturated, aqueous NaHCO3 and additional CH2Cl2. The layers were separated, and the organics were dried with MgSO4 and concentrated. The crude material was purified by silica gel gradient chromatography (0-50% ethyl acetate in hexanes), providing ±benzyl 2-methyl-5-oxopiperidine-1-carboxylate.

후처리

  1. additionwas added dropwise over 5 min at −78° C
  2. customquenched with addition of half-saturated, aqueous NaHCO3 and additional CH2Cl2
  3. customThe layers were separated
  4. dry with materialthe organics were dried with MgSO4
  5. concentrationconcentrated
  6. customThe crude material was purified by silica gel gradient chromatography (0-50% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-a516e98f4dcd4bb2ae8556d61230fd93
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08962611B2

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