HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246837Generated: October 30, 2026
Phosphorus oxychloride → HCID 21906820, compound
https://huagongshe.com/reaction/1246837
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178438985 | HCID 178438985 | — |
| Product | HCID 21906820 | HCID 21906820 | 51% |
Reaction Steps
Then, 4-chloro-6-(4-(2-isopropyl-phenylsulfanyl)-3-trifluoromethyl-phenyl)-pyrimidine 47 was prepared as follows. Compound 46 (1.40 g, 3.59 mmol) was treated with POCl3 (30 mL) at 60° C. for an hour. The reaction mixture was concentrated on a rotor-vapor, and the residue was treated with crushed ice (10 g). Water (50 mL) was added. The aqueous solution was then extracted with ethyl acetate (2×50 mL). The combined organic layers were washed with brine (3×50 mL), dried over MgSO4, filtered and concentrated. The crude product was purified by chromatography to give a brown oil 47 (0.74 g, 51%). 1H-NMR (CDCl3, 400 MHz) δ 1.19 (d, J=6.7 Hz, 6H). 3.50 (heptet, J=6.8 Hz, 1H), 6.89 (d, J=8.5 Hz, 1H), 7.24–7.28 (m, 1H), 7.46–7.50 (m, 2H), 7.54 (d, J=7.6 Hz, 1H), 7.68 (s, 1H), 7.93 (d, J=8.4 Hz, 1H), 8.38 (s, 1H), 9.00(s, 1H). MS (DCI) m/z 409, 411 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129247B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-58e2ff13fdf6468f877b61d7dad28adc |
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| Source note | uspto-grants-2006_10 |
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