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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-1-methylpyridinium iodide | HCID 167069 | — |
| Reactant | 3,4-Dihydro-2H-1,4-benzoxazine | HCID 585096 | — |
| Reactant | 2-(2,5-Dichloro-phenoxy)-nicotinic acid | HCID 16795996 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [2-(2,5-Dichloro-phenoxy)-pyridin-3-yl]-(2,3-dihydro-benzo[1,4]oxazin-4-yl)-methanone | HCID 59294483 | 18.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309734B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-088ecb34b69c4381ac6ae2aa185d75b2 |
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| Source note | uspto-grants-2012_11 |
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