HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400280Generated: October 31, 2026
Phosphorus oxychloride → HCID 86707938, compound
https://huagongshe.com/reaction/2400280
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 86707936 | HCID 86707936 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86707938 | HCID 86707938 | 42.6% |
Reaction Steps
To a solution of 6-[6-fluoro-5-methoxy-2-(thiophen-3-yl)indol-1-ylmethyl]pyridine-2-carboxamide (165 mg) in N,N-dimethylformamide (2.1 mL) was added phosphoryl chloride (0.058 mL) under ice-cooling. This mixture was stirred for 50 minutes. The reaction mixture was quenched with a saturated aqueous sodium hydrogen carbonate solution (10 mL). Ethyl acetate and water were then added to the mixture to separate the organic layer. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: ethyl acetate-hexane) to obtain the title compound (67 mg). 1H-NMR (CDCl3) δ ppm: 3.94 (3H, s), 5.47 (2H, s), 6.62 (1H, s), 6.80 (1H, d, J=8.3 Hz), 6.87 (1H, d, J=11.3 Hz), 7.10-7.30 (3H, m), 7.35-7.45 (1H, m), 7.59 (1H, d, J=7.7 Hz), 7.65-7.75 (1H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796247B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-ac0e99b3c7a7457286dc5fc463d3bc1e |
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| Source note | uspto-grants-2014_08 |
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