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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535437Generated: October 25, 2026

Dicyclohexylcarbodiimide → tert-butyl-N-[1-[[5-[benzenesulfonyl(methyl)amino]-6-(2-phenylethynyl)-pyridin-2-yl]amino]-1-oxopropan-2-yl]-N-methylcarbamate

https://huagongshe.com/reaction/535437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(((Tert-butoxy)carbonyl)(methyl)amino)propanoic acidHCID 4436857—
ReactantN-[6-amino-2-(2-phenylethynyl)pyridin-3-yl]-N-methylbenzenesulfonamideHCID 86694389—
SolventDichloromethaneHCID 6344—
Producttert-butyl-N-[1-[[5-[benzenesulfonyl(methyl)amino]-6-(2-phenylethynyl)-pyridin-2-yl]amino]-1-oxopropan-2-yl]-N-methylcarbamateHCID 86694427—

Reaction Steps

A mixture of 2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]propanoic acid (54 mg, 0.26 mmol) and N,N′-dicyclohexylcarbodiimide (27 mg, 0.13 mmol) in DCM (1.5 ml) is stirred at RT for 20 minutes. This mixture is added to N-[6-amino-2-(2-phenylethynyl)pyridin-3-yl]-N-methylbenzenesulfonamide E5a (16 mg, 0.04 mmol) and DIPEA (9 μl; 0.05 mmol) in DCM (0.5 ml). After stirring for 4 days at 40° C. the reaction mixture is diluted with DCM and extracted with water. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The crude product (22 mg) is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859541B2
Source datasetuspto-grants-2014_10
ORD IDord-3c65ac84661a465ca3e3fd404214d0a6
Source noteuspto-grants-2014_10