HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663497Generated: October 29, 2026
Phosphorus pentachloride → HCID 178526362, compound
https://huagongshe.com/reaction/1663497
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 178522737 | HCID 178522737 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178526362 | HCID 178526362 | 19% |
Reaction Steps
A solution of N-{4-[4-(3-bromo-4-fluorophenyl)-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl]-1,2,5-oxadiazol-3-yl}-1H-tetrazole-5-carboxamide (12 mg, 27 μmol) in pyridine (0.3 mL) was treated with phosphorus pentachloride (13 mg, 60 μmol) at 25° C. The reaction mixture was stirred at 0° C. for 2 h, concentrated, rediluted with toluene and concentrated to a residue. This material was diluted with ethanol (1 mL), treated with sodium cyanoborohydride (5 mg, 82 μmol), and stirred for 2 h. The reaction mixture was concentrated, diluted with ethanol (1 mL), treated with 2.0 M sodium hydroxide in water (0.2 mL), and stirred for 45 min. Purification of the crude reaction mixture by preparative LCMS gave the desired product (2 mg, 19%). LCMS for C11H10BrFN9O2 (M+H)+: m/z=398.0, 400.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034953B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-1060500441b9499e96949d05f4e49008 |
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| Source note | uspto-grants-2011_10 |
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