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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877399Generated: November 2, 2026

Isobutyraldehyde → [2-(2,5-Dichloro-phenoxy)-pyridin-3-yl]-(4-isobutyl-3,4-dihydro-2H-quinoxalin-1-yl)-methanone

https://huagongshe.com/reaction/1877399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyraldehydeHCID 6561—
ReactantDibutyltin dichlorideHCID 12688—
ReactantPhenylsilaneHCID 12752—
Reactant[2-(2,5-Dichloro-phenoxy)-pyridin-3-yl]-(3,4-dihydro-2H-quinoxalin-1-yl)-methanoneHCID 59294486—
SolventDimethylformamideHCID 6228—
Product[2-(2,5-Dichloro-phenoxy)-pyridin-3-yl]-(4-isobutyl-3,4-dihydro-2H-quinoxalin-1-yl)-methanoneHCID 4619512938%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of [2-(2,5-dichloro-phenoxy)-pyridin-3-yl]-(3,4-dihydro-2H-quinoxalin-1-yl)-methanone (24 mg, 0.06 mmol, 1.0 equiv; Example 122) in anhydrous DMF (1 mL) was added 2-methyl-propionaldehyde (17.3 mg, 22 μL, 0.24 mmol, 4.0 equiv; [CAS RN 78-84-2]), dibutyltin dichloride (1.8 mg, 0.006 mmol, 0.1 equiv; [CAS RN 683-18-1]) and phenylsilane (13.0 mg, 15 μL, 0.12 mmol, 2.0 equiv; [CAS RN 694-53-1]). The reaction mixture was heated by microwave irradiation to 150° C. for 15 min. 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 10.3 mg (38%) of the title compound as a light yellow powder. MS (ISP): 456.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309734B2
Source datasetuspto-grants-2012_11
ORD IDord-5e63784e56e74e6aa1f14c38f39b9fb0
Source noteuspto-grants-2012_11