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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678516Generated: November 2, 2026

4-Methylmorpholine → (R)-2-{6-Chloro-4'-[4-(4-(propane-1-sulfonyl)-piperazin-1-ylmethyl)-phenylcarbamoyl]-biphenyl-3-ylcarbamoyl}-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1678516

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-(Propylsulfonyl)piperazin-1-yl)methyl]anilineHCID 28273548—
Reactant(R)-2-(4'-Carboxy-6-chloro-biphenyl-3-ylcarbamoyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 67373093—
SolventDimethylformamideHCID 6228—
Product(R)-2-{6-Chloro-4'-[4-(4-(propane-1-sulfonyl)-piperazin-1-ylmethyl)-phenylcarbamoyl]-biphenyl-3-ylcarbamoyl}-piperidine-1-carboxylic acid tert-butyl esterHCID 67373676—

Reaction Steps

A mixture of (R)-2-(4′-Carboxy-6-chloro-biphenyl-3-ylcarbamoyl)-piperidine-1-carboxylic acid tert-butyl ester (73 mg), 4-(4-(propane-1-sulfonyl)-piperazin-1-ylmethyl)-phenylamine (118 mg) and HBTU (91 mg) in dry DMF (4 ml) containing N-methylmorpholine (52 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-48e1734bab90407986c8be473952b39a
Source noteuspto-grants-2011_08