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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801458Generated: October 30, 2026

Potassium Carbonate → [3-(6-Methoxy-3-nitro-pyridin-2-ylamino)-propyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1801458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl (3-aminopropyl)carbamateHCID 2735700—
Reactant2-Chloro-6-methoxy-3-nitropyridineHCID 2795029—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
Product[3-(6-Methoxy-3-nitro-pyridin-2-ylamino)-propyl]-carbamic acid tert-butyl esterHCID 6863191196.5%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 2-chloro-6-methoxy-3-nitropyridine (5.9 g; commercial), N-(tert-butoxycarbonyl)-1,3-propanediamine (4.48 g; commercial) and K2CO3 (3.55 g) in MeCN (90 mL) and DMF (25 mL) was heated at 40° C. for 30 min. The reaction mixture was filtered and the filtrate was evaporated under reduced pressure. The residue was taken up in EA, sequentially washed with water and brine and evaporated under reduced pressure, affording 8.1 g (96% yield) of a crude yellow solid which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349826B2
Source datasetuspto-grants-2013_01
ORD IDord-556912d0069e4d7fb161e5c767c13ca7
Source noteuspto-grants-2013_01