Thionyl Chloride → [Rac]-4-{2-[2-(4-chloro-phenyl)-4,5,6,7-tetrahydro-2h-indazol-3-yl]-2-cyclohexyl-acetylamino}-3-trifluoromethyl-benzoic acid methyl ester

HRID 1678640Notes

Reaction equation

HRID 1678640 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:16]([CH:17]([CH:21]3[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]3)[C:18](O)=[O:19])=[C:15]3[C:10]([CH2:11][CH2:12][CH2:13][CH2:14]3)=[N:9]2)=[CH:4][CH:3]=1.S(Cl)(Cl)=O.[CH3:31][O:32][C:33](=[O:45])[C:34]1[CH:39]=[CH:38][C:37]([NH2:40])=[C:36]([C:41]([F:44])([F:43])[F:42])[CH:35]=1>CN(C1C=CN=CC=1)C>[CH3:31][O:32][C:33](=[O:45])[C:34]1[CH:39]=[CH:38][C:37]([NH:40][C:18](=[O:19])[CH:17]([C:16]2[N:8]([C:5]3[CH:4]=[CH:3][C:2]([Cl:1])=[CH:7][CH:6]=3)[N:9]=[C:10]3[C:15]=2[CH2:14][CH2:13][CH2:12][CH2:11]3)[CH:21]2[CH2:26][CH2:25][CH2:24][CH2:23][CH2:22]2)=[C:36]([C:41]([F:43])([F:42])[F:44])[CH:35]=1

Participants

5

Reactant 3

HCID 24386Thionyl ChlorideHCID 25067388Methyl 4-amino-3-(trifluoromethyl)benzoateHCID 67131112[2-(4-Chloro-phenyl)-4,5,6,7-tetrahydro-2H-indazol-3-yl]-cyclohexyl-acetic acid

Product 1

HCID 45110773[Rac]-4-{2-[2-(4-chloro-phenyl)-4,5,6,7-tetrahydro-2h-indazol-3-yl]-2-cyclohexyl-acetylamino}-3-trifluoromethyl-benzoic acid methyl ester

Reagents, catalysts & solvents 1

HCID 142844-(Dimethylamino)pyridineCatalyst

Procedure

In analogy to the procedure described in example 6, [2-(4-chloro-phenyl)-4,5,6,7-tetrahydro-2H-indazol-3-yl]-cyclohexyl-acetic acid (example 5.1) was converted into the corresponding acid chloride with thionyl chloride which subsequently reacted with 4-amino-3-trifluoromethyl-benzoic acid methyl ester (CAS Reg. No. 34040-64-7 167760-75-0) in the presence of DMAP to give the title compound as yellow oil. MS: m/e=574.4 [M+H+].

Sources & evidence

ORD record
ord-1044a0e11ae54cfdbd1c235e49f9e7b1
Source dataset
uspto-grants-2011_08
Patent number
US08008505B2

Reaction notes

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