HCID 7667367, compound → HCID 69707347, compound

HRID 991820Notes

Reaction equation

HRID 991820 reaction equation
[N:1]1([S:11]([C:14]2[CH:15]=[C:16]3[C:20](=[CH:21][CH:22]=2)[NH:19][C:18](=[O:23])[CH2:17]3)(=[O:13])=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][CH2:2]1.[O:24]=[C:25]1[C:30]2=[CH:31][NH:32][C:33]([CH:34]=O)=[C:29]2[CH2:28][CH2:27][O:26]1>>[N:1]1([S:11]([C:14]2[CH:15]=[C:16]3[C:20](=[CH:21][CH:22]=2)[NH:19][C:18](=[O:23])[C:17]3=[CH:34][C:33]2[NH:32][CH:31]=[C:30]3[C:25](=[O:24])[O:26][CH2:27][CH2:28][C:29]=23)(=[O:13])=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][CH2:2]1

Participants

3

Reactant 2

HCID 7667367HCID 7667367, compoundHCID 98340494-Oxo-2,4,6,7-tetrahydropyrano[3,4-C]pyrrole-1-carbaldehyde

Product 1

HCID 69707347HCID 69707347, compound

Procedure

5-(3,4-Dihydro-2H-quinoline-1-sulfonyl)-1,3-dihydro-indol-2-one was condensed with 4-oxo-2,4,6,7-tetrahydro-pyrano[3,4-c]pyrrole-1-carbaldehyde to give the title compound.

Sources & evidence

ORD record
ord-a6001dbc20f2423fba571723df0f5ecb
Source dataset
uspto-grants-2002_10
Patent number
US06465507B2

Reaction notes

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