4-[2-(Pyrrolidin-1-yl)ethyl]piperidine → Ammonia

HRID 469119

반응식

HRID 469119 반응식
[CH:1]1([N:4]([CH2:18][C:19]2[N:23]=[C:22]([C:24]([O:26]CC)=O)[O:21][N:20]=2)[S:5]([C:8]2[C:13]([CH3:14])=[CH:12][C:11]([O:15][CH3:16])=[CH:10][C:9]=2[CH3:17])(=[O:7])=[O:6])[CH2:3][CH2:2]1.[N:29]1([CH2:34][CH2:35][CH:36]2[CH2:41][CH2:40][NH:39][CH2:38][CH2:37]2)[CH2:33][CH2:32][CH2:31][CH2:30]1.C[Al](C)C>ClCCCl>[NH3:4].[CH:1]1([N:4]([CH2:18][C:19]2[N:23]=[C:22]([C:24]([N:39]3[CH2:38][CH2:37][CH:36]([CH2:35][CH2:34][N:29]4[CH2:33][CH2:32][CH2:31][CH2:30]4)[CH2:41][CH2:40]3)=[O:26])[O:21][N:20]=2)[S:5]([C:8]2[C:13]([CH3:14])=[CH:12][C:11]([O:15][CH3:16])=[CH:10][C:9]=2[CH3:17])(=[O:6])=[O:7])[CH2:3][CH2:2]1

참가 물질

6

반응물 3

HCID 2962934-[2-(Pyrrolidin-1-yl)ethyl]piperidineHCID 16682925TrimethylaluminumHCID 58393317ethyl 3-({Cyclopropyl[(4-methoxy-2,6-dimethylphenyl)sulfonyl]amino}methyl)-1,2,4-oxadiazole-5-carboxylate

생성물 2

HCID 222AmmoniaHCID 46175639HCID 46175639, 화합물

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

The title compound was prepared according to general procedure AT using ethyl 3-({cyclopropyl[(4-methoxy-2,6-dimethylphenyl)sulfonyl]amino}methyl)-1,2,4-oxadiazole-5-carboxylate (30 mg, 0.07 mmol), 4-[2-(pyrrolidin-1-yl)ethyl]piperidine (29 mg, 0.14 mmol) and trimethylaluminium (2 M in toluene, 0.07 mL) in DCE (5 mL). A portion of the crude product was purified using FCC, eluting with 95:4.5:0.5 DCM:MeOH:NH3, to afford the title compound.

후처리

  1. customThe title compound was prepared
  2. customA portion of the crude product was purified
  3. washeluting with 95:4.5:0.5 DCM

출처 및 근거

ORD 기록
ord-55b7629596d048c9aa2921dbb093b487
출처 데이터셋
uspto-grants-2014_01
특허 번호
US08623859B2

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