HCID 12903423, compound → HCID 131712632, compound

HRID 1703338Notes

Reaction equation

HRID 1703338 reaction equation
O[C:2]1C=C(O)C=C2C=1C(=O)CCN2.[CH3:14][O:15][C:16]1[CH:21]=[C:20]([CH2:22][NH:23][CH2:24][CH2:25][CH2:26][NH:27][CH2:28][CH2:29][CH2:30][CH2:31][NH:32][CH2:33][CH2:34][CH2:35][NH2:36])[CH:19]=[CH:18][C:17]=1[OH:37].[OH:38][N:39]1[C:48]2[C:43](=[CH:44][CH:45]=[C:46]([O:49][CH:50]([CH2:52][CH2:53][CH2:54][CH2:55][CH3:56])[CH3:51])[CH:47]=2)[C:42](=[O:57])[CH2:41][CH2:40]1>>[CH3:14][O:15][C:16]1[CH:21]=[C:20]([CH2:22][NH:23][CH2:24][CH2:25][CH2:26][NH:27][CH2:28][CH2:29][CH2:30][CH2:31][NH:32][CH2:33][CH2:34][CH2:35][NH2:36])[CH:19]=[CH:18][C:17]=1[OH:37].[OH:38][N:39]1[C:48]2[C:43](=[CH:44][CH:45]=[C:46]([O:49][CH:50]([CH2:52][CH2:53][CH2:54][CH2:55][CH3:56])[CH3:51])[CH:47]=2)[C:42](=[O:57])[CH2:41][CH:40]1[CH3:2]

Participants

3

Reactant 2

HCID 12903423HCID 12903423, compoundHCID 131712634HCID 131712634, compound

Product 1

HCID 131712632HCID 131712632, compound

Procedure

In like manner, 5,7-dihydroxy-4-oxo-1,2,3,4-tetrahydroquinoline converted to dl-5-hydroxy-7-(2-heptyloxy)-4-oxo-1,2,3,4-tetrahydroquinoline, an oil.

Sources & evidence

ORD record
ord-ab9b3c30014744baa9053ea220147036
Source dataset
uspto-grants-1982_09
Patent number
US04351833

Reaction notes

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