Phenylacetic Acid → HCID 58168005, compound

HRID 1029258Notes

Reaction equation

HRID 1029258 reaction equation
[C:1]([N:9]1[CH2:12][CH:11]([NH:13][C:14]2[CH:23]=[CH:22][N:21]=[C:20]3[C:15]=2[C:16]2[CH:28]=[CH:27][CH:26]=[CH:25][C:17]=2[C:18](=[O:24])[NH:19]3)[CH2:10]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:29]1(CC(O)=O)C=CC=CC=1>>[C:7]1([CH2:2][C:1]([N:9]2[CH2:12][CH:11]([NH:13][C:14]3[CH:23]=[CH:22][N:21]=[C:20]4[C:15]=3[C:16]3[CH:28]=[CH:27][CH:26]=[CH:25][C:17]=3[C:18](=[O:24])[NH:19]4)[CH2:10]2)=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:29]=1

Participants

3

Reactant 2

HCID 999Phenylacetic AcidHCID 58168313HCID 58168313, compound

Product 1

HCID 58168005HCID 58168005, compound

Procedure

The title compound was synthesized according to the procedure described for the preparation of Example 360 using the amine intermediate from example 366 and phenylacetic acid to provide 368. LC-MS (M+H=385, obsd.=385).

Workup

  1. customThe title compound was synthesized

Sources & evidence

ORD record
ord-48477246680f49b9ac6719ef1315487c
Source dataset
uspto-grants-2014_05
Patent number
US08735584B2

Reaction notes

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