2-Naphthoic acid → HCID 709437, compound

HRID 1837152Notes

Reaction equation

HRID 1837152 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([O:14][CH3:15])[C:11]=1[O:12][CH3:13])[C:6]([OH:8])=O.[NH2:16][C:17]1[CH:18]=[CH:19][C:20]([O:23][CH3:24])=[N:21][CH:22]=1.C1C2C(=CC=CC=2)C=CC=1C(O)=O.IC1C=CC(N)=CC=1>>[CH3:15][O:14][C:10]1[CH:9]=[C:5]([CH:4]=[C:3]([O:2][CH3:1])[C:11]=1[O:12][CH3:13])[C:6]([NH:16][C:17]1[CH:22]=[N:21][C:20]([O:23][CH3:24])=[CH:19][CH:18]=1)=[O:8]

Participants

5

Reactant 4

HCID 71232-Naphthoic acidHCID 83573,4,5-Trimethoxybenzoic AcidHCID 108934-IodoanilineHCID 811216-Methoxy-3-pyridinylamine

Product 1

HCID 709437HCID 709437, compound

Procedure

This compound was synthesized by the same procedure as for Example 15, except 3,4,5-trimethoxybenzoic acid and 5-amino-2-methoxypyridine were used instead of 2-napthoic acid and 4-iodoaniline. Tiny off-white needles. M+319.3

Sources & evidence

ORD record
ord-7f36277f15a0407eb6d52617e59b4c92
Source dataset
uspto-grants-2004_08
Patent number
US06780883B2

Reaction notes

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