Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 68831233 | HCID 68831233 | — |
| Product | HCID 18009485 | HCID 18009485 | — |
Reaction Steps
To a solution of 1-hydroxy-1-acetoxymethyl)-4-phenyl-4-(3-(2-methoxyphenyl)-3-oxo-2-azaprop-1-yl)-cyclohexane (Example 171, isomer #1, 19.5 mg, 0.047 mmol) in 2 mL of pyridine was added SOCl2 (0.2 mL, 2.7 mmol) at 0° C. and the mixture was stirred at rt for 1 h. It was then poured into NaHCO3, extracted with CH2Cl2 (2×), dried over MgSO4 filtered and concentrated. The residue was purified by HPLC (Waters RCM, μ Porosil, 25 mm×10 cm) using a mixture of (5:4:1 hexane-methyl tert-butyl ether-acetonitrile:hexane, 7.75/6.0 mL/min) to give the title compound. 1H NMR (CDCl3) δ 8.18 (d, 1H, J=7.8 Hz), 7.60 (bs, 1H), 7.26-7.41 (m, 6H), 7.03 (t, 1H, J=7.6 Hz), 6.83 (d, 1H, J=8.3 Hz), 5.81 (s, 1H), 4.39-4.45 (m, 2H), 3.80 (d of d, 1H, J=6.4, 13.2 Hz), 3.75 (d of d, 1H, J=6.4, 13.2 Hz), 3.15 (s, 3H), 2.61 (d, 1H, J=17.7 Hz), 2.38 (d, 1H, J=17.7), 2.04 (s, 3H), 1.77-2.16 (m, 4H); Mass Spectrum (CI) m/e 394 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06632836B1 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-9054c6a7ef194ec5920a5ee17e8c6dc0 |
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| Source note | uspto-grants-2003_10 |
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