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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877356Generated: October 31, 2026

Triethylamine → [2-(2,5-Dichloro-phenoxy)-pyridin-3-yl]-(2,3-dihydro-benzo[1,4]oxazin-4-yl)-methanone

https://huagongshe.com/reaction/1877356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
Reactant3,4-Dihydro-2H-1,4-benzoxazineHCID 585096—
Reactant2-(2,5-Dichloro-phenoxy)-nicotinic acidHCID 16795996—
SolventDichloromethaneHCID 6344—
Product[2-(2,5-Dichloro-phenoxy)-pyridin-3-yl]-(2,3-dihydro-benzo[1,4]oxazin-4-yl)-methanoneHCID 5929448318.3%

Reaction Steps

To a solution of 2-(2,5-dichloro-phenoxy)-nicotinic acid (42.6 mg, 0.15 mmol, 1.0 equiv; Example 31, Step 1) in dichloromethane (1.5 mL) was added 3,4-dihydro-2H-benzo[1,4]oxazine (22.9 mg, 0.17 mmol, 1.1 equiv; [CAS RN 5735-53-5]), triethylamine (30.4 mg, 42 μL, 0.3 mmol, 2.0 equiv; [CAS RN 121-44-8]) and 2-chloro-1-methylpyridinium iodide (42.2 mg, 0.17 mmol, 1.1 equiv; [CAS RN 14338-32-0]). The reaction mixture was stirred at rt over night. Removal of the solvent mixture under reduced pressure and purification by preparative HPLC on reversed phase (Xterra® PrepMSC 18, 5 μm, 19×50 mm column equipped with a Gilson Liquid Handler 215 autosampler, two Rainin Dynamax® SD-300 pumps, a Sedex ELSD 75 lightscatter and a Dionex UVD 340S UV detector) eluting with a gradient of acetonitrile/water provided 11 mg (18%) of the title compound. MS (ISP): 401.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309734B2
Source datasetuspto-grants-2012_11
ORD IDord-088ecb34b69c4381ac6ae2aa185d75b2
Source noteuspto-grants-2012_11