N-(3-Aminopropyl)morpholine → HCID 135987551, compound

HRID 2079871Notes

Reaction equation

HRID 2079871 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](O)=[O:40])[CH:34]=1)C1C=CC=CC=1.[NH2:42][CH2:43][CH2:44][CH2:45][N:46]1[CH2:51][CH2:50][O:49][CH2:48][CH2:47]1>>[N:46]1([CH2:45][CH2:44][CH2:43][NH:42][C:39]([C:35]2[CH:34]=[C:33]([C:10]3[CH:11]=[C:12]([C:23]4[N:27]([CH2:28][CH2:29][CH2:30][O:31][CH3:32])[N:26]=[N:25][N:24]=4)[C:13]([OH:15])=[CH:14][C:9]=3[OH:8])[CH:38]=[CH:37][CH:36]=2)=[O:40])[CH2:51][CH2:50][O:49][CH2:48][CH2:47]1

Participants

3

Reactant 2

HCID 61055N-(3-Aminopropyl)morpholineHCID 57695565HCID 57695565, compound

Product 1

HCID 135987551HCID 135987551, 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 N-(3-aminopropyl) morpholine as described in general procedure D. LCMS: 497 [M+H].

Workup

  1. customThis product was synthesized

Sources & evidence

ORD record
ord-bc265b21fdb04ec3b41ae7eb029ebb90
Source dataset
uspto-grants-2011_04
Patent number
US07932279B2

Reaction notes

Loading…