Furan-2-acetic acid → HCID 58189255, compound

HRID 1423159Notes

Reaction equation

HRID 1423159 reaction equation
[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][C:7]([OH:9])=O.[CH2:10]([C@@H:17]1[NH:22][CH2:21][CH2:20][N:19]([C:23]2[CH:28]=[CH:27][C:26]([O:29][CH3:30])=[C:25]([O:31][CH:32]3[CH2:35][CH2:34][CH2:33]3)[CH:24]=2)[CH2:18]1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>>[CH2:10]([C@H:17]1[CH2:18][N:19]([C:23]2[CH:28]=[CH:27][C:26]([O:29][CH3:30])=[C:25]([O:31][CH:32]3[CH2:35][CH2:34][CH2:33]3)[CH:24]=2)[CH2:20][CH2:21][N:22]1[C:7](=[O:9])[CH2:6][C:2]1[O:1][CH:5]=[CH:4][CH:3]=1)[C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1

Participants

3

Reactant 2

HCID 75974Furan-2-acetic acidHCID 58188985HCID 58188985, compound2×

Product 1

HCID 58189255HCID 58189255, compound

Procedure

Prepared by the method outlined for Example 189 using furan-2-yl-acetic acid and 3(S)-benzyl-1-(3-cyclobutoxy-4-methoxy-phenyl)-piperazine (Example 7, Compound 95) as starting materials. Product as an oil. LC/MS (Method B) 2.77 min, [M+1]+ 461. Potency class B.

Workup

  1. customPrepared by the method
  2. customLC/MS (Method B) 2.77 min, [M+1]+ 461

Sources & evidence

ORD record
ord-a5e904e23db64587932fd5589530abaa
Source dataset
uspto-grants-2015_01
Patent number
US08927546B2

Reaction notes

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