4-Benzyloxyphenylacetic acid → HCID 178456454, compound

HRID 2056253Notes

Reaction equation

HRID 2056253 reaction equation
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][C:16]([OH:18])=O)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:19]([N:22]1[C:31](=[O:32])[C:30]2[NH:29][C:28]([C:33]3[N:37]([CH3:38])[N:36]=[C:35]([NH2:39])[CH:34]=3)=[N:27][C:26]=2[N:25]([CH2:40][CH2:41][CH3:42])[C:23]1=[O:24])[CH2:20][CH3:21]>>[CH3:42][CH2:41][CH2:40][N:25]1[C:23](=[O:24])[N:22]([CH2:19][CH2:20][CH3:21])[C:31](=[O:32])[C:30]2[C:26]1=[N:27]/[C:28](/[N:29]=2)=[C:33]1/[CH:34]=[C:35]([NH:39][C:16]([CH2:15][C:12]2[CH:11]=[CH:10][C:9]([O:8][CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)=[CH:14][CH:13]=2)=[O:18])[NH:36][N:37]/1[CH3:38]

Participants

3

Procedure

Using 4-(benzyloxy)phenylacetic acid and 1,3-dipropyl-8-(3-amino-1-methylpyrazol-5-yl)xanthine (Example 1, Compound AS3).

Sources & evidence

ORD record
ord-032a9e4b98fa4b259ec07c6d1e945bff
Source dataset
uspto-grants-2008_02
Patent number
US07335655B2

Reaction notes

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