1-(2-Chloroethyl)pyrrolidine hydrochloride → [4-(2-Pyrrolidin-1-yl-ethoxy)-2-trifluoromethyl-phenyl]-(5-thiophen-3-yl-thiazol-2-yl)-amine

HRID 1713689Notes

Reaction equation

HRID 1713689 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]1[CH2:56][CH2:55][CH2:54][CH2:53]1>C(Cl)Cl.CO>[N:52]1([CH2:51][CH2:50][O:43][C:40]2[CH:41]=[CH:42][C:37]([NH:36][C:34]3[S:35][C:31]([C:28]4[CH:29]=[CH:30][S:26][CH:27]=4)=[CH:32][N:33]=3)=[C:38]([C:44]([F:47])([F:46])[F:45])[CH:39]=2)[CH2:56][CH2:55][CH2:54][CH2:53]1

Participants

5

Reactant 3

HCID 816681-(2-Chloroethyl)pyrrolidine hydrochlorideHCID 11245147{5-[4-(3-Dimethylamino-propoxy)-phenyl]-thiazol-2-yl}phenyl-amineHCID 589235234-(5-Thiophen-3-yl-thiazol-2-ylamino)-3-trifluoromethyl-phenol

Product 1

HCID 58923519[4-(2-Pyrrolidin-1-yl-ethoxy)-2-trifluoromethyl-phenyl]-(5-thiophen-3-yl-thiazol-2-yl)-amine

Reagents, catalysts & solvents 1

HCID 21226129Dichloromethane methanolSolvent

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 1-(2-chloroethyl)-pyrrolidine hydrochloride. The title compound: ES-MS: 439.9 [M+H]+; single peak at tR=3.36 min (System 2); Rf=0.22 (CH2Cl2/MeOH, 90/10).

Workup

  1. customThe title compound is prepared

Sources & evidence

ORD record
ord-4300a1aa59d4410bbd75dfe2d70364fc
Source dataset
uspto-grants-2010_09
Patent number
US07795288B2

Reaction notes

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