Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Methyl-1,2,3,4-tetrahydroquinoline | HCID 96289 | — |
| Reactant | HCID 67367227 | HCID 67367227 | — |
| Product | HCID 59294516 | HCID 59294516 | 21.3% |
Reaction Steps
A solution of 2-(3-chloro-4-fluoro-phenoxy)-5-fluoro-nicotinic acid (34.3 mg, 0.12 mmol, 1.0 equiv; Example 86, Step 1) in thionyl chloride (492 mg, 300 μL, 4.14 mmol, 34.5 equiv; [CAS RN 7719-09-7]) was heated to 100° C. over night. The reaction mixture was concentrated under reduced pressure, remaining thionyl chloride removed by azotropic distillation with toluene and the residue dissolved in anhydrous DMF (1 mL). To this solution was added N-ethyldiisopropylamine (155 mg, 204 μL, 1.20 mmol, 10.0 equiv; [CAS RN 7087-68-5]) and 2-methyl-1,2,3,4-tetrahydro-quinoline (22.1 mg, 0.15 mmol, 1.25 equiv; [CAS RN 1780-19-4]) and the reaction mixture heated by microwave irradiation to 100° C. for 20 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 10.6 mg (21%) of the title compound. MS (ISP): 414.9 [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-df2a0476cffb42eaa59e16ee61754bd5 |
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| Source note | uspto-grants-2012_11 |
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