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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678519Generated: November 1, 2026

4-Methylmorpholine → ({6-Chloro-4'[4-(4-methanesulfonyl-piperazin-1-ylmethyl)-phenylcarbamoyl]-biphenyl-3-ylcarbamoyl}-methyl)-methyl-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1678519

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant4-(4-Methanesulfonyl-piperazin-1-ylmethyl)-phenylamineHCID 11369231—
Reactant5'-[2-(tert-Butoxycarbonyl-methyl-amino)-acetylamino]-2'-chloro-biphenyl-4-carboxylic acidHCID 67374495—
SolventDimethylformamideHCID 6228—
Product({6-Chloro-4'[4-(4-methanesulfonyl-piperazin-1-ylmethyl)-phenylcarbamoyl]-biphenyl-3-ylcarbamoyl}-methyl)-methyl-carbamic acid tert-butyl esterHCID 67374257—

Reaction Steps

A mixture of 5′-[2-(tert-Butoxycarbonyl-methyl-amino)-acetylamino]-2′-chloro-biphenyl-4-carboxylic acid (85 mg), 4-(4-methanesulfonyl-piperazin-1-ylmethyl)-phenylamine (81 mg) and HBTU (120 mg) in dry DMF (4 ml) containing N-methylmorpholine (65 μl) was stirred at room temp for 18 h.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008303B2
Source datasetuspto-grants-2011_08
ORD IDord-8c3895e1e6254cb5a666bb2afba9a799
Source noteuspto-grants-2011_08