HCID 10173378, compound → HCID 22346591, compound

HRID 897412Notes

Reaction equation

HRID 897412 reaction equation
Cl[C:2]1[C:7]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([C:14]([F:17])([F:16])[F:15])[CH:9]=2)=[C:6]([C:18]2[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=2)[N:5]=[C:4]([CH2:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[N:3]=1.FC1C=CC(C2C3N([CH:61]=[N:62][N:63]=3)C(NC(C3C=CC=CC=3)(C)C)=NC=2C2C=CN=CC=2)=CC=1>>[C:26]1([CH2:25][CH2:24][C:4]2[N:3]3[CH:61]=[N:62][N:63]=[C:2]3[C:7]([C:8]3[CH:13]=[CH:12][CH:11]=[C:10]([C:14]([F:16])([F:15])[F:17])[CH:9]=3)=[C:6]([C:18]3[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=3)[N:5]=2)[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1

Participants

3

Reactant 2

HCID 10173378HCID 10173378, compoundHCID 22346623HCID 22346623, compound

Product 1

HCID 22346591HCID 22346591, compound

Procedure

The title compound was synthesized from 4-chloro-2-(2-phenylethyl)-6-(4-pyridyl)-5-(3-(trifluoromethyl)phenyl)pyrimidine in the same manner as 2-(8-(4-fluorophenyl)-7-(4-pyridyl)-1,2,4-triazolo[4,3-c]pyrimidin-5-yl)amino-2-phenylpropane; MS m/z (M+H)+ 446; C25H18F3N5 requir. 445.4.

Sources & evidence

ORD record
ord-e112ae1723234b5ebcb8568630aff699
Source dataset
uspto-grants-2005_07
Patent number
US06921762B2

Reaction notes

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