3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid → N-(2-(2-(4-Chlorophenyl)oxazol-4-yl)-2-methylpropyl)-3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide

Participants

Role	Name	HCID	Charge
Reactant	3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid	HCID 25180854	—
Reactant	2-(2-(4-Chlorophenyl)oxazol-4-yl)-2-methylpropan-1-amine	HCID 67325623	—
Product	N-(2-(2-(4-Chlorophenyl)oxazol-4-yl)-2-methylpropyl)-3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzamide	HCID 67324866	14%

Reaction Steps

This compound was synthesized from 2-(2-(4-chlorophenyl)oxazol-4-yl)-2-methylpropan-1-amine and 3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid as described in example 8 step 6 (8 mg, yield 14%). 1H NMR (CDCl3) δ 8.59 (t, J=1.7 Hz, 1H), 8.25 (d, J=7.9 Hz, 1H), 8.12 (d, J=6.7 Hz, 1H), 7.99 (d, J=6.6 Hz, 2H), 7.64 (t, J=7.7 Hz, 2H) 7.49 (s, 1H), 7.38 (d, J=4.9 Hz, 1H), 2.03 (s, 2H), 1.40 (s, 6H). MS (ESI) m/z: Calculated for C23H18ClF3N4O3: 490.10. found: 491.1 (M+H)+.

Provenance & Evidence

DOI	10.6084/m9.figshare.5104873.v1
Patent number	US08901156B2
Source dataset	uspto-grants-2014_12
ORD ID	ord-57b61a702e3348efae42471a1aa47f21
Source note	uspto-grants-2014_12