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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389663Generated: October 25, 2026

1-Bromo-4-((methylsulfonyl)methyl)benzene → tert-Butyl{4-[(4'-methanesulfonylmethyl-4-methoxy-biphenyl-3-ylmethyl)-amino]-cyclohexyl}-methyl-carbamate

https://huagongshe.com/reaction/2389663

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-((methylsulfonyl)methyl)benzeneHCID 2761415—
Reactant3-{[4-(BOC-methyl-amino)-cyclohexylamino]-methyl}-4-methoxy-benzene boronic acidHCID 25208191—
Producttert-Butyl{4-[(4'-methanesulfonylmethyl-4-methoxy-biphenyl-3-ylmethyl)-amino]-cyclohexyl}-methyl-carbamateHCID 59683471—

Reaction Steps

Boronic acid 4 (200 mg, 0.51 mmol) is coupled to aryl bromide 197 (127 mg, 0.51 mmol) using Method A. On filtration of the cooled reaction mixture through celite and removal of the solvents in vacuo, the crude residue obtained is used in the next synthetic step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273747B2
Source datasetuspto-grants-2012_09
ORD IDord-1d10fab51f554a0c97d1b6b2915508bc
Source noteuspto-grants-2012_09