HCID 70277252, compound → HCID 23296445, compound

HRID 1954401Notes

Reaction equation

HRID 1954401 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([O:9][CH2:10][C:11]2[CH:20]=[C:19]([CH3:21])[C:18]3[C:13](=[CH:14][C:15]([N:22]([S:29]([C:32]4[CH:33]=[CH:34][CH:35]=[C:36]5[C:41]=4[N:40]=[CH:39][CH:38]=[CH:37]5)(=[O:31])=[O:30])[CH2:23][C:24]([O:26][CH2:27][CH3:28])=[O:25])=[CH:16][CH:17]=3)[N:12]=2)=[CH:5][CH:4]=1)#[N:2].[ClH:42].C(=O)([O-])[O-].[NH4+:47].[NH4+]>C(O)C>[ClH:42].[C:1]([C:3]1[CH:8]=[CH:7][C:6]([O:9][CH2:10][C:11]2[CH:20]=[C:19]([CH3:21])[C:18]3[C:13](=[CH:14][C:15]([N:22]([S:29]([C:32]4[CH:33]=[CH:34][CH:35]=[C:36]5[C:41]=4[N:40]=[CH:39][CH:38]=[CH:37]5)(=[O:30])=[O:31])[CH2:23][C:24]([O:26][CH2:27][CH3:28])=[O:25])=[CH:16][CH:17]=3)[N:12]=2)=[CH:5][CH:4]=1)(=[NH:47])[NH2:2]

Participants

4

Reactant 2

HCID 70277252HCID 70277252, compoundHCID 86755731HCID 86755731, compound

Product 1

HCID 23296445HCID 23296445, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

Prepared analogously to Example 1e from 2-[(4-cyanophenyl)-oxymethyl]-4-methyl-7-[N-(ethoxycarbonylmethyl)-quinoline-8-sulphonylamino)-quinoline and hydrochloric acid/ammonium carbonate in ethanol.

Sources & evidence

ORD record
ord-5199e12f1c794bf782aacf01981852ea
Source dataset
uspto-grants-2000_09
Patent number
US06121308

Reaction notes

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