Diisopropylethylamine → HCID 178459300, compound

HRID 2053344Notes

Reaction equation

HRID 2053344 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.[OH:20][C:21]([CH3:25])([CH3:24])[CH2:22][NH2:23].CCN(C(C)C)C(C)C>>[OH:20][C:21]([CH3:25])([CH3:24])[CH2:22][NH:23][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

Participants

4

Reactant 3

HCID 81531DiisopropylethylamineHCID 951022-Propanol, 1-amino-2-methyl-HCID 58585737(5Z)-2-(methylthio)-5-(6-quinolinylmethylidene)-1,3-thiazol-4(5H)-one

Product 1

HCID 178459300HCID 178459300, compound

Procedure

Then 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-hydroxy-2-methyl-propylamine and DIEA to give 2-(2-hydroxy-2-methyl-propylamino)-5-[1-quinolin-6-yl-meth-(Z)-ylidene]-thiazol-4-one. LC-MS m/e 328 (MH+).

Sources & evidence

ORD record
ord-7d4c09b8668c46d8b315f8399f00fe65
Source dataset
uspto-grants-2008_02
Patent number
US07326786B2

Reaction notes

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