TFMPP hydrochloride → 1-[5-Methyl-1-(2-pyrimidinyl)-4-pyrazolyl]-3-[4-(3-trifluoromethylphenyl)-1-piperazinyl]-1-trans-propene hydrochloride

HRID 1458982Notes

Reaction equation

HRID 1458982 reaction equation
[ClH:1].[CH3:2][C:3]1[N:7]([C:8]2[N:13]=[CH:12][CH:11]=[CH:10][N:9]=2)[N:6]=[CH:5][C:4]=1[C:14](=O)[CH2:15][CH2:16][N:17]1[CH2:26][CH2:25]C2[C:19](=CC=CC=2)[CH2:18]1.Cl.CC1N(C2N=CC=CN=2)N=CC=1/C=C/CN1CCC2C(=CC=CC=2)C1.Cl.[F:55][C:56]([F:70])([F:69])[C:57]1[CH:58]=[C:59]([N:63]2CCNCC2)[CH:60]=[CH:61][CH:62]=1>>[ClH:1].[CH3:2][C:3]1[N:7]([C:8]2[N:9]=[CH:10][CH:11]=[CH:12][N:13]=2)[N:6]=[CH:5][C:4]=1/[CH:14]=[CH:15]/[CH2:16][N:17]1[CH2:18][CH2:19][N:63]([C:59]2[CH:60]=[CH:61][CH:62]=[C:57]([C:56]([F:55])([F:69])[F:70])[CH:58]=2)[CH2:25][CH2:26]1

Participants

4

Reactant 3

HCID 3084246TFMPP hydrochlorideHCID 220973011-[5-Methyl-1-(2-pyrimidinyl)-4-pyrazolyl]-3-(1,2,3,4-tetrahydroisoquinolin-2-yl)-1-propanone hydrochlorideHCID 220973051-[5-Methyl-1-(2-pyrimidinyl)-4-pyrazolyl]-3-(1,2,3,4-tetrahydroisoquinolin-2-yl)-1-trans-propene hydrochloride

Product 1

HCID 220972821-[5-Methyl-1-(2-pyrimidinyl)-4-pyrazolyl]-3-[4-(3-trifluoromethylphenyl)-1-piperazinyl]-1-trans-propene hydrochloride

Procedure

The procedures of Example 6 (1) and (2) were repeated but substituting the 1,2,3,4-tetrahydroisoquinoline hydrochloride employed in Example 6 (1) by 730 mg of 1-(3-trifluoromethylphenyl)piperazine hydrochloride. After the completion of the post treatment, 75 mg of the title compound was obtained.

Sources & evidence

ORD record
ord-50bb966d161d489a956ce29cece50e58
Source dataset
uspto-grants-1998_12
Patent number
US05852019

Reaction notes

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