2-Chloroethyldiisopropylammonium chloride → [4-(2-Diisopropylamino-ethoxy)-2-trifluoromethyl-phenyl]-(5-thiophen-3-yl-thiazol-2-yl)-amine
Reaction equation
CN(C)CCCOC1C=CC(C2SC(NC3C=CC=CC=3)=NC=2)=CC=1.[S:26]1[CH:30]=[CH:29][C:28]([C:31]2[S:35][C:34]([NH:36][C:37]3[CH:42]=[CH:41][C:40]([OH:43])=[CH:39][C:38]=3[C:44]([F:47])([F:46])[F:45])=[N:33][CH:32]=2)=[CH:27]1.Cl.Cl[CH2:50][CH2:51][N:52]([CH:56]([CH3:58])[CH3:57])[CH:53]([CH3:55])[CH3:54]>C(Cl)Cl.CO>[CH:53]([N:52]([CH:56]([CH3:58])[CH3:57])[CH2:51][CH2:50][O:43][C:40]1[CH:41]=[CH:42][C:37]([NH:36][C:34]2[S:35][C:31]([C:28]3[CH:29]=[CH:30][S:26][CH:27]=3)=[CH:32][N:33]=2)=[C:38]([C:44]([F:47])([F:46])[F:45])[CH:39]=1)([CH3:55])[CH3:54]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound is prepared as described in Example 8 for {5-[4-(3-dimethylamino-propoxy)-phenyl]-thiazol-2-yl}phenyl-amine but starting from 4-(5-thiophen-3-yl-thiazol-2-ylamino)-3-trifluoromethyl-phenol (Example 28) and using (2-chloroethyl)-diisopropylamine hydrochloride. The title compound: ES-MS: 469.9 [M+H]+; single peak at tR=3.67 min (System 2); Rf=0.38 (CH2Cl2/MeOH, 90/10).
Workup
- customThe title compound is prepared
Sources & evidence
- ORD record
- ord-35ef7f08960743b58cdc1607196788f7
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07795288B2
Reaction notes
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