HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401307Generated: October 30, 2026
Phosphorus pentachloride → HCID 69937333, compound
https://huagongshe.com/reaction/2401307
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | HCID 14978323 | HCID 14978323 | — |
| Solvent | Phosphorus oxychloride | HCID 24813 | — |
| Product | HCID 69937333 | HCID 69937333 | — |
Reaction Steps
To a suspension of cyclopentanecarboxylic acid (6-amino-2,4-dioxo-3-propyl-1,2,3,4-tetrahydro-pyrimidin-5-yl)-amide (0.40 g, crude) obtained from step 1 in phosphorus oxychloride (25 ml) was added phosphorus pentachloride (0.10 g) and the resulting reaction mixture was refluxed overnight. Phosphorus oxychloride was evaporated under reduced pressure. The residue was slowly quenched with water. Ethyl acetate was added and the organic layer was separated and washed thoroughly with water followed by brine. The ethyl acetate layer was dried over anhydrous sodium sulphate and concentrated under vacuum. The crude product was purified by preparative TLC using dichloromethane, methanol (9:1) as the solvent system to give 0.075 g (19% over two steps) of the product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796290B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-690ae2856deb4856aaa758cf170276a7 |
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| Source note | uspto-grants-2014_08 |
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