1,2-Dichloroethane → n-[(1r)-1-[(3,4-Dichlorophenyl)methyl]-2-(4-{2-[(methylsulfonyl)amino]phenyl}piperazinyl)-2-oxoethyl]((3s)(3-1,2,3,4-tetrahydroisoquinolyl))-carboxamide

HRID 1242733노트

반응식

HRID 1242733 반응식
Cl.[CH3:2][S:3]([NH:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[N:13]1[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]1)(=[O:5])=[O:4].[CH3:19][C:20]([O:23][C:24]([NH:26][C@@H:27]([C:37]([OH:39])=[O:38])[CH2:28][C:29]1[CH:34]=[CH:33][C:32]([Cl:35])=[C:31]([Cl:36])[CH:30]=1)=[O:25])([CH3:22])[CH3:21].CC[N:42]([CH:46]([CH3:48])C)[CH:43]([CH3:45])C.C(Cl)CCl.[CH:53]1[CH:58]=N[C:56]2N(O)N=N[C:55]=2[CH:54]=1>CN(C=O)C>[Cl:36][C:31]1[CH:30]=[C:29]([CH2:28][C@@H:27]([NH:26][C:24]([O:23][C:20]([CH3:22])([CH3:21])[CH3:19])=[O:25])[C:37]([N:16]2[CH2:17][CH2:18][N:13]([C:8]3[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=3[NH:6][S:3]([CH3:2])(=[O:4])=[O:5])[CH2:14][CH2:15]2)=[O:38])[CH:34]=[CH:33][C:32]=1[Cl:35].[Cl:36][C:31]1[CH:30]=[C:29]([CH2:28][C@@H:27]([NH:26][C:24]([C@@H:46]2[CH2:48][C:56]3[C:45](=[CH:58][CH:53]=[CH:54][CH:55]=3)[CH2:43][NH:42]2)=[O:25])[C:37]([N:16]2[CH2:17][CH2:18][N:13]([C:8]3[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=3[NH:6][S:3]([CH3:2])(=[O:4])=[O:5])[CH2:14][CH2:15]2)=[O:39])[CH:34]=[CH:33][C:32]=1[Cl:35]

참가 물질

8

실험 절차

N-[(1R)-1-[(3,4-Dichlorophenyl)methyl]-2-(4-{2-[(methylsulfonyl)amino]phenyl}piperazinyl)-2-oxoethyl](tert-butoxy)carboxamide was prepared according to the procedure for Preparation XIX using (methylsulfonyl)(2-piperazinylphenyl)amine hydrochloride (800 mg, 2.8 mmol), N-Boc-D-3,4-dichlorophenylalanine (930 mg, 2.80 mmol) (Peptech), DIEA (480 μl, 2.80 mmol), EDC (1.66 g, 5.60 mmol), HOAT (400 mg, 3.0 mmol) and DMF (10 mL). The crude product was purified by flash chromatography (SiO2, 1:1 hexane:EtOAc) and concentrated in vacuo to afford the desired compound (1.0 g). MS (ESI, pos. ion) m/z: 571 (M+H), (ESI, neg. ion) m/z: 569 (M−H). Calc'd for C25H32Cl2N4O5S: 570.15.

후처리

  1. customThe crude product was purified by flash chromatography (SiO2, 1:1 hexane:EtOAc)
  2. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-c7d3d40ed73745b5a345fbf909da5db3
출처 데이터셋
uspto-grants-2006_10
특허 번호
US07115607B2

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