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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224145Generated: October 31, 2026

4-Bromo-2-fluoroaniline → Jtp-70902

https://huagongshe.com/reaction/2224145

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-fluoroanilineHCID 123050—
ReactantHCID 59717043HCID 59717043—
ProductJtp-70902HCID 1152718683.1%

Reaction Conditions

Temperature135 °C

Reaction Steps

To toluene-4-sulfonic acid 3-cyclopropyl-1-(3-methanesulfonylaminophenyl)-8-methyl-2,4,7-trioxo-1,2,3,4,7,8-hexahydropyrido[2,3-d]pyrimidin-5-yl ester 15 (3.5 g) obtained in Step 8 was added 2-fluoro-4-bromoaniline 16 (23 g), and the mixture was stirred under heating at 135° C. for 3 hrs. The reaction mixture was purified by column chromatography (chloroform:acetone=9:1) to give N-{3-[5-(4-bromo-2-fluoro-phenylamino)-3-cyclopropyl-8-methyl-2,4,7-trioxo-3,4,7,8-tetrahydro-2H-pyrido[2,3-d]pyrimidin-1-yl]phenyl}-methanesulfonamide 17 (3.0 g, 83%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378423B2
Source datasetuspto-grants-2008_05
ORD IDord-4fbf845094ff4c6896177ac66d9a50fd
Source noteuspto-grants-2008_05