Methyl iodide → HCID 46847611, compound

HRID 1044329Notes

Reaction equation

HRID 1044329 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:17](=[O:18])[C:16]3[C:11](=[CH:12][CH:13]=[N:14][C:15]=3[NH:19][CH2:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[NH:10][CH:9]=2)=[CH:4][CH:3]=1.IC.[CH:29]1([CH2:32]Br)[CH2:31][CH2:30]1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[C:17](=[O:18])[C:16]3[C:11](=[CH:12][CH:13]=[N:14][C:15]=3[NH:19][CH2:20][C:21]3[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=3)[N:10]([CH2:32][CH:29]3[CH2:31][CH2:30]3)[CH:9]=2)=[CH:6][CH:7]=1

Participants

4

Reactant 3

HCID 6328Methyl iodideHCID 81503BromomethylcyclopropaneHCID 46847351HCID 46847351, compound

Product 1

HCID 46847611HCID 46847611, compound

Procedure

The title compound was prepared as described in Example 2 above except that 3-(4-chlorophenyl)-1,4-dihydro-4-oxo-5-(2-phenethylamino)-1,6-naphthyridine was replaced with 3-(4-chlorophenyl)-1,4-dihydro-4-oxo-5-benzylamino-1,6-naphthyridine and iodomethane was replaced with cyclopropylmethyl bromide. MS 426 (M+1)+.

Sources & evidence

ORD record
ord-aae20c21942b4f37bd3dab28d6c0ba62
Source dataset
uspto-grants-2013_10
Patent number
US08563579B2

Reaction notes

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