HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877414Generated: October 26, 2026
Ethyl 3-bromopropionate → 3-{4-[2-(2,5-Dichloro-phenoxy)-5-fluoro-pyridine-3-carbonyl]-3,4-dihydro-2H-quinoxalin-1-yl}-propionic acid ethyl ester
https://huagongshe.com/reaction/1877414
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 3-bromopropionate | HCID 68320 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | [2-(2,5-Dichloro-phenoxy)-5-fluoro-pyridin-3-yl]-(3,4-dihydro-2H-quinoxalin-1-yl)-methanone | HCID 59294514 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-{4-[2-(2,5-Dichloro-phenoxy)-5-fluoro-pyridine-3-carbonyl]-3,4-dihydro-2H-quinoxalin-1-yl}-propionic acid ethyl ester | HCID 59294481 | 8% |
Reaction Steps
To a solution of [2-(2,5-dichloro-phenoxy)-5-fluoro-pyridin-3-yl]-(3,4-dihydro-2H-quinoxalin-1-yl)-methanone (25.1 mg, 0.06 mmol, 1.0 equiv; Example 147) in anhydrous DMF (1 mL) was added lithium aluminium hydride (2.3 mg, 0.06 mmol, 1.0 equiv; [CAS RN 16853-85-3]) and the reaction mixture stirred at rt. After 30 min, 3-bromo-propionic acid ethyl ester (13.0 mg, 10 μL, 0.072 mmol, 1.2 equiv; [CAS RN 539-74-2]) was added and the reaction mixture heated by microwave irradiation to 150° C. for 30 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 2.4 mg (8%) of the title compound as a light brown oil. MS (ISP): 518.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08309734B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-0b5c8d4b7d5749259c6d283c0a831aad |
|---|
| Source note | uspto-grants-2012_11 |
|---|