Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Chloro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile | HCID 57926113 | — |
| Reactant | HCID 67155049 | HCID 67155049 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69937824 | HCID 69937824 | 6.1% |
Reaction Steps
To the solution of 2-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile (409 mg, 1.55 mmol), 3-(3-Bromo-5-fluoro-pyridin-4-yl)-oxetan-3-ol (350 mg, 1.41 mmol) and PdCl2(dppf).CH2Cl2 adduct (115 mg, 0.141 mmol) in DMF (7 mL) was added a solution of Na2CO3 (2M in water, 1.76 ml, 3.53 mmol) under Nitrogen atmosphere. The mixture was stirred and heated at 100° C. for 4 hrs. After letting cool to room temperature, solvent was removed in vacuo. The resulting residue was dissolved in DCM and saturated NH4Cl solution. After extraction with DCM and separation, the combined extracts were concentrated and purified by ISCO 12 g (0-40%, v/v, EtOAc/Heptane) to give 2-Chloro-4-[5-fluoro-4-(3-hydroxy-oxetan-3-yl)-pyridin-3-yl]-benzonitrile (26 mg, 6%) as colorless solid; ESI-MS m/z: 305 [M++1]+, Retention time 1.27 min; 1H-NMR (CDCl3, 400 MHz) δ 4.42 (d, J=8.4 Hz, 2H), 4.66 (d, J=8.4 Hz, 2H), 7.57 (d, J=6.8 Hz, 1H), 7.76 (s, 1H), 7.80 (d, J=6.8 Hz, 1H), 8.41 (s, 1H), 8.59 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08519134B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-830cffc46ea54f5c9b21056d8d10c40d |
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| Source note | uspto-grants-2013_08 |
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