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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026894Generated: November 1, 2026

Methanesulfonamide → N-[7-(3-Fluorobenzylamino)-6-(4-phenylpiperidine-1-carbonyl)pyrazolo[1,5-a]pyrimidine-3-carbonyl]methanesulfonamide

https://huagongshe.com/reaction/1026894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonamideHCID 72879—
Reactant7-(3-Fluorobenzylamino)-6-(4-phenylpiperidine-1-carbonyl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acidHCID 67540477—
ProductN-[7-(3-Fluorobenzylamino)-6-(4-phenylpiperidine-1-carbonyl)pyrazolo[1,5-a]pyrimidine-3-carbonyl]methanesulfonamideHCID 67540529—

Reaction Steps

In the same manner as in Example 1, step 6 and using 7-(3-fluorobenzylamino)-6-(4-phenylpiperidine-1-carbonyl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (0.09 g, 0.18 mmol) obtained in step 2 and methanesulfonamide (0.1 g, 1.08 mmol), compound a-6 (0.06 g, 64%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729264B2
Source datasetuspto-grants-2014_05
ORD IDord-167fed640e9f4f3b9c2697bd8ef9ae37
Source noteuspto-grants-2014_05