HCID 178494663, compound → HCID 178494662, compound

HRID 1488006Notes

Reaction equation

HRID 1488006 reaction equation
[CH3:1][O:2][CH2:3][C:4]1[NH:5][C:6]([C:10]2[C:11](C)=[CH:12][C:13](C)=[C:14]([CH:31]=2)[C:15]([N:17]2[CH2:22][CH2:21][CH:20]([C:23]3[CH:30]=[CH:29][C:26]([C:27]#[N:28])=[CH:25][CH:24]=3)[CH2:19][CH2:18]2)=[O:16])=[C:7]([CH3:9])[N:8]=1.COCC1NC(C2C=C(C=CC=2)C(O)=O)=C(C)N=1.COCC1NC(C2C(C)=CC(C)=C(C=2)C(O)=O)=C(C)N=1>>[CH3:1][O:2][CH2:3][C:4]1[NH:5][C:6]([C:10]2[CH:31]=[C:14]([CH:13]=[CH:12][CH:11]=2)[C:15]([N:17]2[CH2:18][CH2:19][CH:20]([C:23]3[CH:24]=[CH:25][C:26]([C:27]#[N:28])=[CH:29][CH:30]=3)[CH2:21][CH2:22]2)=[O:16])=[C:7]([CH3:9])[N:8]=1

Participants

4

Procedure

The title compound was prepared using standard chemical manipulations and procedures similar to those used for the preparation of compound 2, except 3-(2-(methoxymethyl)-4-methyl-1H-imidazol-5-yl)benzoic acid (compound 156.1) was used in place of 5-(2-(methoxymethyl)-4-methyl-1H-imidazol-5-yl)-2,4-dimethylbenzoic acid (compound 2.3). m/z (ES+) 415 (M+H)+.

Sources & evidence

ORD record
ord-003054d605f94985ab5010bb45034cbc
Source dataset
uspto-grants-2016_08
Patent number
US09428502B2

Reaction notes

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