4-Aminobenzoic Acid → HCID 178456460, compound

HRID 2056259Notes

Reaction equation

HRID 2056259 reaction equation
[NH2:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.[CH2:11]([N:14]1[C:23](=[O:24])[C:22]2[NH:21][C:20]([C:25]3[N:29]([CH3:30])[N:28]=[C:27]([O:31][CH2:32][C:33](O)=[O:34])[CH:26]=3)=[N:19][C:18]=2[N:17]([CH2:36][CH2:37][CH3:38])[C:15]1=[O:16])[CH2:12][CH3:13]>>[CH3:38][CH2:37][CH2:36][N:17]1[C:15](=[O:16])[N:14]([CH2:11][CH2:12][CH3:13])[C:23](=[O:24])[C:22]2[C:18]1=[N:19]/[C:20](/[N:21]=2)=[C:25]1/[CH:26]=[C:27]([O:31][CH2:32][C:33]([NH:1][C:2]2[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=2)=[O:34])[NH:28][N:29]/1[CH3:30]

Participants

3

Reactant 2

HCID 9784-Aminobenzoic AcidHCID 135610069HCID 135610069, compound

Product 1

HCID 178456460HCID 178456460, compound

Procedure

Using 4-(amino)benzoic acid and 2-[5-(1,3-dipropyl-xanthin-8-yl)-1-methylpyrazol-3-yloxy]acetic acid (Example 36), according to the method described in Example 36.

Sources & evidence

ORD record
ord-3d77e0084ab04a1ab27cb8e59132ad93
Source dataset
uspto-grants-2008_02
Patent number
US07335655B2

Reaction notes

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