Ethyl Acetate → (R)-1-[2-[3-(3,4-dichloro-phenyl)-1-(3,4,5-trimethoxy-benzoyl)-pyrrolidin-3-yl]-ethyl]-4-(pyridin-3-yl)-piperidine-4-carboxylic acid morpholine-amide

HRID 400080Notes

Reaction equation

HRID 400080 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:28]=[C:29]([O:33][CH3:34])[C:30]=1[O:31][CH3:32])[C:6]([N:8]1[CH2:12][CH2:11][C@@:10]([CH2:21][CH2:22]CS([O-])(=O)=O)([C:13]2[CH:18]=[CH:17][C:16]([Cl:19])=[C:15]([Cl:20])[CH:14]=2)[CH2:9]1)=[O:7].[N:35]1([C:41]([NH2:43])=[O:42])[CH2:40][CH2:39][O:38][CH2:37][CH2:36]1.[N:44]1[CH:49]=[CH:48][CH:47]=[C:46]([C:50]2([C:56]([OH:58])=[O:57])[CH2:55][CH2:54][NH:53][CH2:52][CH2:51]2)[CH:45]=1.C(OCC)(=O)C>CO.ClCCl>[N:35]1([C:41]([NH2:43])=[O:42])[CH2:40][CH2:39][O:38][CH2:37][CH2:36]1.[Cl:20][C:15]1[CH:14]=[C:13]([C@@:10]2([CH2:21][CH2:22][N:53]3[CH2:52][CH2:51][C:50]([C:46]4[CH:45]=[N:44][CH:49]=[CH:48][CH:47]=4)([C:56]([OH:58])=[O:57])[CH2:55][CH2:54]3)[CH2:11][CH2:12][N:8]([C:6](=[O:7])[C:5]3[CH:28]=[C:29]([O:33][CH3:34])[C:30]([O:31][CH3:32])=[C:3]([O:2][CH3:1])[CH:4]=3)[CH2:9]2)[CH:18]=[CH:17][C:16]=1[Cl:19]

Participants

5

Procedure

Prepare by the method of Example 88.6 using (S)-2-[1-(3,4,5-trimethoxy-benzoyl)-3-(3,4-dichloro-phenyl)-pyrrolidin-3-yl]-ethyl-methanesulfonate and 4-(pyridin-3-yl)-piperidine-4-carboxylic acid morpholine-amide to give, after chromatography on silica gel eluting sequentially with ethyl acetate, 2% methanol/dichloromethane, 5% methanol/dichloromethane, and then 7% methanol/dichloromethane, the title compound: Rf =0.44 (silica gel, methanol/dichloromethane/concentrated ammonia 10/90/0.5).

Workup

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Sources & evidence

ORD record
ord-23adedcd145e4e5a8709f64b5163efb9
Source dataset
uspto-grants-1998_10
Patent number
US05824690

Reaction notes

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