Anthranilic Acid → HCID 22724754, compound

HRID 279210Notes

Reaction equation

HRID 279210 reaction equation
[O:1]=[C:2]1[C:11](/[CH:12]=[CH:13]/[C:14](Cl)=[O:15])=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[O:3]1.[C:17]([OH:26])(=[O:25])[C:18]1[C:19](=[CH:21][CH:22]=[CH:23][CH:24]=1)[NH2:20].C(N(CC)CC)C>O1CCCC1>[C:17]([C:18]1[CH:24]=[CH:23][CH:22]=[CH:21][C:19]=1[NH:20][C:14](=[O:15])/[CH:13]=[CH:12]/[C:11]1[C:2](=[O:1])[O:3][C:4]2[C:9]([CH:10]=1)=[CH:8][CH:7]=[CH:6][CH:5]=2)([OH:26])=[O:25]

Participants

5

Reactant 3

HCID 227Anthranilic AcidHCID 8471TriethylamineHCID 88041898HCID 88041898, compound

Product 1

HCID 22724754HCID 22724754, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Prepared analogously to Example 31 from trans-3-(2-oxo-2H-chromen-3-yl)-acrylic acid chloride and anthranilic acid in tetrahydrofuran with the addition of triethylamine.

Sources & evidence

ORD record
ord-674241a406a74a62b253cd97f017fb25
Source dataset
uspto-grants-2002_03
Patent number
US06362210B1

Reaction notes

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