N-Methylcyclohexylamine → HCID 178518090, compound

HRID 2053362Notes

Reaction equation

HRID 2053362 reaction equation
CS[C:3]1[S:4]/[C:5](=[CH:9]\[C:10]2[CH:11]=[C:12]3[C:17](=[CH:18][CH:19]=2)[N:16]=[CH:15][CH:14]=[CH:13]3)/[C:6](=[O:8])[N:7]=1.[CH2:20]1[CH2:25][CH2:24][CH2:23][CH2:22][CH:21]1NC.C[CH2:29][N:30](C(C)C)C(C)C>>[CH:21]1([CH2:29][NH:30][C:3]2[S:4]/[C:5](=[CH:9]\[C:10]3[CH:11]=[C:12]4[C:17](=[CH:18][CH:19]=3)[N:16]=[CH:15][CH:14]=[CH:13]4)/[C:6](=[O:8])[N:7]=2)[CH2:22][CH2:23][CH2:24][CH2:25][CH2:20]1

Participants

4

Reactant 3

HCID 7514N-MethylcyclohexylamineHCID 81531DiisopropylethylamineHCID 58585737(5Z)-2-(methylthio)-5-(6-quinolinylmethylidene)-1,3-thiazol-4(5H)-one

Product 1

HCID 178518090HCID 178518090, compound

Procedure

Similar procedure as described in example 1b was used, starting from 2-methylsulfanyl-5-[1-quinolin-6-yl-meth-(Z)-ylidene]-thiazol-4-one, 2-cyclohexyl-methylamine and DIEA to give 2-(cyclohexylmethyl-amino)-5-[1-quinolin-6-yl-meth-(Z)-ylidene]-thiazol-4-one. LC-MS m/e 352 (MH+).

Sources & evidence

ORD record
ord-db499d745d594b5d96f2d6eef90f5bcc
Source dataset
uspto-grants-2008_02
Patent number
US07326786B2

Reaction notes

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