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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19604Generated: October 26, 2026

7-Methanesulfonyl-5-(4'-methoxy-biphenyl-3-yl)-pyrazolo[1,5-c]pyrimidine → (4-{4-[5-(4'-Methoxy-biphenyl-3-yl)-pyrazolo[1,5-c]pyrimidin-7-ylamino]-phenylcarbamoyl}-benzyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/19604

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Methanesulfonyl-5-(4'-methoxy-biphenyl-3-yl)-pyrazolo[1,5-c]pyrimidineHCID 67317653—
Reactant[4-(4-Amino-phenylcarbamoyl)-benzyl]-carbamic acid tert-butyl esterHCID 67319189—
Product(4-{4-[5-(4'-Methoxy-biphenyl-3-yl)-pyrazolo[1,5-c]pyrimidin-7-ylamino]-phenylcarbamoyl}-benzyl)-carbamic acid tert-butyl esterHCID 67319203—

Reaction Conditions

Temperature130 °C

Reaction Steps

Under an inert gas atmosphere at 130° C. bath temperature is heated neat a mixture of 7-methanesulfonyl-5-(4′-methoxy-biphenyl-3-yl)-pyrazolo[1,5-c]pyrimidine and [4-(4-amino-phenylcarbamoyl)-benzyl]-carbamic acid tertbutyl ester (compound B3) overnight. The crude product is purified by silica gel flash chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745446B2
Source datasetuspto-grants-2010_06
ORD IDord-4b05f3aff05e4cd38be34cf9b4a03da6
Source noteuspto-grants-2010_06