2-(2-Aminoethyl)-1-methylpyrrolidine → HCID 135987503, compound

HRID 2079872Notes

Reaction equation

HRID 2079872 reaction equation
C([O:8][C:9]1[CH:14]=[C:13]([O:15]CC2C=CC=CC=2)[C:12]([C:23]2[N:27]([CH2:28][CH2:29][CH2:30][O:31][CH3:32])[N:26]=[N:25][N:24]=2)=[CH:11][C:10]=1[C:33]1[CH:38]=[CH:37][CH:36]=[C:35]([C:39]([OH:41])=O)[CH:34]=1)C1C=CC=CC=1.[NH2:42][CH2:43][CH2:44][CH:45]1[CH2:49][CH2:48][CH2:47][N:46]1[CH3:50]>>[CH3:50][N:46]1[CH2:47][CH2:48][CH2:49][CH:45]1[CH2:44][CH2:43][NH:42][C:39]([C:35]1[CH:34]=[C:33]([C:10]2[CH:11]=[C:12]([C:23]3[N:27]([CH2:28][CH2:29][CH2:30][O:31][CH3:32])[N:26]=[N:25][N:24]=3)[C:13]([OH:15])=[CH:14][C:9]=2[OH:8])[CH:38]=[CH:37][CH:36]=1)=[O:41]

Participants

3

Reactant 2

HCID 983882-(2-Aminoethyl)-1-methylpyrrolidineHCID 57695565HCID 57695565, compound

Product 1

HCID 135987503HCID 135987503, compound

Procedure

This product was synthesized using 2′,4′-bis-benzyloxy-5′-[1-(3-methoxy-propyl)-1H-tetrazol-5-yl]-biphenyl-3-carboxylic acid and 2-(2-aminoethyl)-1-methylpyrrolidine as described in general procedure D. LCMS: 481 [M+H].

Workup

  1. customThis product was synthesized

Sources & evidence

ORD record
ord-1a8723c35cb24fac91cfbde481f3eaab
Source dataset
uspto-grants-2011_04
Patent number
US07932279B2

Reaction notes

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