2-Naphthoic acid → HCID 8796093, compound

HRID 1837148Notes

Reaction equation

HRID 1837148 reaction equation
[CH2:1]([S:8][C:9]1[CH:17]=[CH:16][CH:15]=[CH:14][C:10]=1[C:11]([OH:13])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:18][O:19][C:20]1[CH:26]=[CH:25][C:23]([NH2:24])=[CH:22][CH:21]=1.C1C2C(=CC=CC=2)C=CC=1C(O)=O.IC1C=CC(N)=CC=1>>[CH2:1]([S:8][C:9]1[CH:17]=[CH:16][CH:15]=[CH:14][C:10]=1[C:11]([NH:24][C:23]1[CH:25]=[CH:26][C:20]([O:19][CH3:18])=[CH:21][CH:22]=1)=[O:13])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

5

Reactant 4

HCID 71232-Naphthoic acidHCID 7732P-AnisidineHCID 108934-IodoanilineHCID 2641822-(Benzylsulfanyl)benzoic acid

Product 1

HCID 8796093HCID 8796093, compound

Procedure

The title compound was synthesized by the same procedure as for Example 15, except 2-benzylsulfanyl-benzoic acid and 4-methoxyaniline were used instead of 2-napthoic acid and 4-iodoaniline. M+364.2

Sources & evidence

ORD record
ord-343958911a164020bde5a170ee4a2c74
Source dataset
uspto-grants-2004_08
Patent number
US06780883B2

Reaction notes

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