Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272180Generated: October 31, 2026

2-Chlorobenzoyl chloride → N-[5-(5-chloro-2-methylbenzoxazol-6-yl)(2-pyridyl)](2-chlorophenyl)carboxamide

https://huagongshe.com/reaction/2272180

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzoyl chlorideHCID 69110—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium bicarbonate methylene chlorideHCID 23716255—
Reactant5-(5-Chloro-2-methylbenzoxazol-6-yl)-2-pyridylamineHCID 58487024—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-[5-(5-chloro-2-methylbenzoxazol-6-yl)(2-pyridyl)](2-chlorophenyl)carboxamideHCID 5848690471%

Reaction Steps

To a solution of 5-(5-chlorob-2-methylenzoxazol-6-yl)-2-pyridylamine (36) (19 mg, 0.073 mmol) and 2 mg DMAP in 2 ml DCM was added 2-chlorobenzoyl chloride (19 μl, 0.14 mmol) followed by addition of DIEA (64 μl). The resulting solution was stirred at r.t. for overnight. The reaction mixture was worked up with aq. NaHCO3/DCM. DCM phase was washed with brine, concentrated to dryness. The residue was dissolved in 2 ml THF/MeOH/H2O (5:4:1) and stirred with 1N NaOH (140 μl) at r.t. for 1 h before worked up with EA/aq. NaHCO3. Silica gel flash chromatography furnished 20.6 mg 37 as pale yellow solid. (yield: 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120751B2
Source datasetuspto-grants-2015_09
ORD IDord-c5dfafc5647a4fe6869accfec769f17c
Source noteuspto-grants-2015_09