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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350778Generated: October 31, 2026

n-Boc-4-(2-cyclopropyl-4-hydroxymethyl-2h-pyrazol-3-yl)-piperidine → N-Boc-4-(2-cyclopropyl-4-formyl-2H-pyrazol-3-yl)-piperidine

https://huagongshe.com/reaction/1350778

Reaction equation

Participants

RoleNameHCIDCharge
Reactantn-Boc-4-(2-cyclopropyl-4-hydroxymethyl-2h-pyrazol-3-yl)-piperidineHCID 21097374—
CatalystManganese dioxideHCID 14801—
SolventTetrahydrofuranHCID 8028—
ProductN-Boc-4-(2-cyclopropyl-4-formyl-2H-pyrazol-3-yl)-piperidineHCID 2109737370.7%

Reaction Steps

The above acid (300 mg, 0.894 mmol) was dissolved in 5 mL of THF. To this solution was added 3.58 mL (3.58 mmol) of 1M borane in THF. After stirring for 5 h, the mixture was poured into 15 mL of 5% HCl. The solution was extracted with 200 mL of EtOAc, and the extract was washed with saturated NaHCO3 and brine, dried over MgSO4, filtered, concentrated, and chromatographed (10–100 EtOAc in hexanes) to give 120 mg of N-Boc-4-(2-cyclopropyl-4-hydroxymethyl-2H-pyrazol-3-yl)-piperidine. This alcohol (100 mg, 0.31 mmol) was stirred overnight in 10 mL of THF with 270 mg (3.1 mmol) of activated MnO2. The mixture was filtered and concentrated to provide 70 mg of N-Boc-4-(2-cyclopropyl-4-formyl-2H-pyrazol-3-yl)-piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214802B2
Source datasetuspto-grants-2007_05
ORD IDord-a98884386ee8443f9d944dec4fafc305
Source noteuspto-grants-2007_05