Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178508874 | HCID 178508874 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 87740010 | HCID 87740010 | — |
Reaction Steps
A mixture of Example 45C (0.56 g, 2.1 mmol) in CHCl3 (4.2 mL) was treated with POCl3 (0.97 mL, 10.5 mmol), cooled to 0° C., treated with triethylamine (0.59 mL, 4.2 mmol), stirred at ambient temperature for 4 hours, diluted with CHCl3 (5 mL), treated with a stream of HCl gas for 2 minutes, stirred at ambient temperature overnight and partitioned between cold 1 M NaOH (50 mL) and CH2Cl2 (50 mL). The layers were separated and the aqueous was extracted with CH2Cl2 (2×50 mL). The combined CH2Cl2 layers were dried (MgSO4), filtered, concentrated under reduced pressure and chromatographed eluting with CH2Cl2 and then 9:1 CH2Cl2:EtOAc to provide the title compound. 1H NMR (DMSO-d6) δ 2.87 (t, J=5.76 Hz, 2H) 4.43 (t, J=5.93 Hz, 2H) 7.12 (s, 2H) 7.15 (d, J=8.81 Hz, 1H) 7.52 (dd, J=8.65, 2.88 Hz, 1H) 7.88 (d, J=2.71 Hz, 1H); MS (M+H)+ m/z 282.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735411B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-f8721110281047f989172dcec334d032 |
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| Source note | uspto-grants-2014_05 |
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