HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523734Generated: November 2, 2026
Phosphorus oxychloride → HCID 71534484, compound
https://huagongshe.com/reaction/1523734
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 86724908 | HCID 86724908 | — |
| Reactant | HCID 86724919 | HCID 86724919 | — |
| Product | HCID 71534484 | HCID 71534484 | 30% |
Reaction Steps
To the mixture of 1-isopropyl-1H-indazole-3-carboxylic acid hydrazide (120 mg, 0.55 mmol) and (1-cyclobutyl piperidin-4-yl) acetic acid hydrochloride (147 mg, 0.74 mmol, obtained in preparation 6) cooled at 0° C., was added phosphoryl chloride (1.5 mL). The reaction temperature was gradually raised to 100° C. and stirred was 2 hours. Upon completion of the reaction, it was cooled to 0° C. and triturated with hexanes (3×25 mL). The crude product was cooled to 0° C., basified with aqueous sodium hydroxide solution and extracted with 5% methanol in dichloromethane. The combined organic layer was dried over anhydrous sodium sulphate and the solvent was removed under reduced pressure. The crude product was purified by silica gel column chromatography to obtain 3-[5-(1-cyclobutyl piperidin-4-yl methyl)-[1,3,4]oxadiazol-2-yl]-1-isopropyl-1H-indazole (62 mg)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09079894B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-8a8c841d850245b3a9871b4159ef359a |
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| Source note | uspto-grants-2015_07 |
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