Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 22485770 | HCID 22485770 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20781264 | HCID 20781264 | 99.7% |
Reaction Steps
To a solution of the amide of Example 44 (80 mg, 0.16 mmol) in toluene (10 ml) under nitrogen was added thionyl chloride (23 μL, 0.32 mmol) and a catalytic amount of dimethylformamide. After refluxing for 16 h, the reaction was cooled to ambient temperature, diluted with water and extracted with ethyl acetate The combined organic layers were washed with brine, dried (MgSO4) and evaporated to give a residue (78 mg) which was purified using preparative thin layer chromatography eluting with ethyl acetate:hexane 1:2 to give the desired product (42 mg). 1H NMR (CDCl3) 7.39-7.31 (4H, m), 7.08-7.04 (2H, m), 6.88-6.84 (1H, m), 6.24 (1H, d, J=6.1 Hz), 4.12 (2H, s), 3.09-3.07 (1H, m), 2.62-2.46 (4H, m), 2.11-2.04 (2H, m), 1.65-1.57 (2H, m). M/z(ES−)=487/489
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06890956B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-4d8f579f47cf476eb44fbee0580ca2d5 |
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| Source note | uspto-grants-2005_05 |
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