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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026922Generated: November 1, 2026

4-(4-Methylphenyl)piperidine hydrochloride → 7-Benzylamino-3-bromo-6-[4-(4-methylphenyl)piperidine-1-carbonyl]pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1026922

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Methylphenyl)piperidine hydrochlorideHCID 20351543—
Reactant7-Benzylamino-3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylic acidHCID 67540363—
Product7-Benzylamino-3-bromo-6-[4-(4-methylphenyl)piperidine-1-carbonyl]pyrazolo[1,5-a]pyrimidineHCID 6754037677%

Reaction Steps

In the same manner as in Example 21, step 5 and using 7-benzylamino-3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylic acid (0.20 g, 0.58 mmol) obtained in Example 22, step 3 instead of 7-benzylamino-3-ethoxycarbonylpyrazolo[1,5-a]pyrimidine-6-carboxylic acid and 4-(4-methylphenyl)piperidine hydrochloride (0.15 g, 0.69 mmol), the title compound (0.22 g, 77%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729264B2
Source datasetuspto-grants-2014_05
ORD IDord-7c328449a9534ff3b361c6479a06541f
Source noteuspto-grants-2014_05