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Potassium Carbonate → N-(3-Methoxycarbonylphenyl)-N-(ethanesulfonyl)pyrid-3-ylmethylamine

HRID 392427
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HRID 392427 반응식
[CH3:1][O:2][C:3]([C:5]1[CH:6]=[C:7]([NH:11][CH2:12][C:13]2[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=2)[CH:8]=[CH:9][CH:10]=1)=[O:4].[CH2:19]([S:21](Cl)(=[O:23])=[O:22])[CH3:20].C(=O)([O-])[O-].[K+].[K+]>ClC(Cl)C.N1C=CC=CC=1>[CH3:1][O:2][C:3]([C:5]1[CH:6]=[C:7]([N:11]([CH2:12][C:13]2[CH:14]=[N:15][CH:16]=[CH:17][CH:18]=2)[S:21]([CH2:19][CH3:20])(=[O:23])=[O:22])[CH:8]=[CH:9][CH:10]=1)=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 11430Potassium CarbonateHCID 11667Ethanesulfonyl chlorideHCID 43139315Methyl 3-((pyridin-3-ylmethyl)amino)benzoate

생성물 1

HCID 23521670N-(3-Methoxycarbonylphenyl)-N-(ethanesulfonyl)pyrid-3-ylmethylamine수율 49%

시약·촉매·용매 2

HCID 1049Pyridine용매
HCID 6365
1,1-Dichloroethane
용매

실험 절차

Into a 0° C. solution of N-(3-methoxycarbonylphenyl) pyrid-3-ylmethylamine (204 g, 0.842 mole, 1 eq) in dichloroethane (3610 mL) and pyridine (1775 mL) was added ethanesulfonyl chloride (114 mL, 1.2 mole, 1.43 eq). The reaction was allowed to warm to room temperature overnight. The dark red reaction was stirred with potassium carbonate (204 g) for 30 minutes and then filtered and concentrated to dryness. The residue was purified by Biotage, eluting with 3:1 to 2:1 DCM/EtOAc mixture to give the title compound as a white solid (137.0 g, 49% yield).

후처리

  1. customThe dark red reaction
  2. filtrationfiltered
  3. concentrationconcentrated to dryness
  4. customThe residue was purified by Biotage
  5. washeluting with 3:1 to 2:1 DCM/EtOAc mixture

출처 및 근거

ORD 기록
ord-32fc6db824284f9f91ed2dd5ed977606
출처 데이터셋
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06800651B2

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