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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085296Generated: October 30, 2026

tert-butyl N-(4-aminobutyl)carbamate → Tert-butyl 4-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]butylcarbamate

https://huagongshe.com/reaction/2085296

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-aminobutyl)carbamateHCID 4351—
ReactantTriethylamineHCID 8471—
Reactant2,4-Dichloro-5,6-dimethyl-3-nitropyridineHCID 12109123—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]butylcarbamateHCID 1210912448%

Reaction Steps

A solution of tert-butyl 4-aminobutylcarbamate (8.52 g, 45.24 mmol) in N,N-dimethylformamide was added to a solution of 2,4-dichloro-5,6-dimethyl-3-nitropyridine (10.00 g, 45.24 mmol) and triethylamine (12.6 mL, 90.5 mmol) in N,N-dimethylformamide (320 mL). The reaction mixture was stirred overnight and then concentrated under reduced pressure. The residue was partitioned between water and ethyl acetate. The layers were separated and the aqueous layer was extracted with ethyl acetate. The organics were combined, washed with brine and then concentrated under reduced pressure to provide a brown oily residue. This material was purified by flash chromatography (400 mL silica gel, eluting initially with 10% ethyl acetate in hexane and then increasing the gradient to 15% and then to 25%) to provide 8.1 g of tert-butyl 4-[(2-chloro-5,6-dimethyl-3-nitropyridin-4-yl)amino]butylcarbamate as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06720334B2
Source datasetuspto-grants-2004_04
ORD IDord-516c5f3fc2524cbb9ae972eec29a2b8e
Source noteuspto-grants-2004_04