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HCID 13927192, compound → HCID 12002365, compound

HRID 563841
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Reaction equation

HRID 563841 reaction equation
CO[C:3]1[CH:22]=[CH:21][C:6]([CH2:7][C:8]([C:10]2[C:11](=[O:20])[O:12][C:13]3[C:18]([CH:19]=2)=[CH:17][CH:16]=[CH:15][CH:14]=3)=[O:9])=[CH:5][CH:4]=1.COC1C=CC(CC(C2C(=O)OC3C(C=2)=C(OC)C=C(OC)C=3)=O)=CC=1.COC1C=CC(CC(C2C(=O)OC3C(C=2)=CC([N+]([O-])=O)=CC=3[N+]([O-])=O)=O)=CC=1.COC1C=CC(CC(C2C(=O)OC3C(C=2)=CC(Br)=CC=3)=O)=CC=1.COC1C=CC(CC(C2C(=O)OC3C(C=2)=CC([Cl:119])=CC=3)=O)=CC=1.COC1C=CC(CC(C2C(=O)OC3C(C=2)=CC=C(OC)C=3)=O)=CC=1.COC1C=CC(CC(C2C(=O)OC3C(C=2)=CC=C(O)C=3)=O)=CC=1>>[Cl:119][C:3]1[CH:22]=[CH:21][C:6]([CH2:7][C:8]([C:10]2[C:11](=[O:20])[O:12][C:13]3[C:18]([CH:19]=2)=[CH:17][CH:16]=[CH:15][CH:14]=3)=[O:9])=[CH:5][CH:4]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

8

Reactant 7

HCID 13927192HCID 13927192, compoundHCID 13927196HCID 13927196, compoundHCID 86635721HCID 86635721, compoundHCID 86635722HCID 86635722, compoundHCID 86635723HCID 86635723, compoundHCID 86635724HCID 86635724, compound
HCID 86635725
HCID 86635725, compound

Product 1

HCID 12002365HCID 12002365, compound

Procedure

Additional preferred compounds according to the second embodiment of compounds according to Formula IA include: 3-(4-methoxybenzylcarbonyl)-2H-chromen-2-one; 3-(4-methoxybenzylcarbonyl)-5,7-dimethoxy-2H-chromen-2-one; 3-(4-methoxybenzylcarbonyl)-6,8-dinitro-2H-chromen-2-one; 3-(4-methoxybenzylcarbonyl)-6-bromo-2H-chromen-2-one; 3-(4-methoxybenzylcarbonyl)-6-chloro-2H-chromen-2-one; 3-(4-methoxybenzylcarbonyl)-7-methoxy-2H-chromen-2-one; 3-(4-methoxybenzylcarbon-yl)-7-hydroxy-2H-chromen-2-one; mixtures thereof; and salts thereof.

Sources & evidence

ORD record
ord-13ce8057367e42b187be7953ae828573
Source dataset
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08067461B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes