1,2,3,4-Tetrahydroquinoline → HCID 22252322, compound

HRID 1611996Notes

Reaction equation

HRID 1611996 reaction equation
[NH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][CH2:2]1.[CH2:11]1[N:16]([CH2:17][CH2:18][CH2:19][C:20](O)=[O:21])[CH2:15][CH2:14][N:13]2[CH2:23][CH2:24][CH2:25][CH2:26][CH:12]12>>[N:1]1([C:20](=[O:21])[CH2:19][CH2:18][CH2:17][N:16]2[CH2:15][CH2:14][N:13]3[CH2:23][CH2:24][CH2:25][CH2:26][CH:12]3[CH2:11]2)[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 694601,2,3,4-TetrahydroquinolineHCID 22252364HCID 22252364, compound

Product 1

HCID 22252322HCID 22252322, compound

Procedure

The procedure is as for Example 2 using as substrate 3,4-dihydro-2H-quinoline and the compound obtained in Step B of Example 2.

Sources & evidence

ORD record
ord-277c7db8727446afa743b85b23046fee
Source dataset
uspto-grants-2006_01
Patent number
US06992085B2

Reaction notes

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