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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173165Generated: November 1, 2026

Triethylamine → N-[2-amino-5-(2-thienyl)phenyl]-6-(2,7-diazaspiro[3.5]non-7-yl)nicotinamide

https://huagongshe.com/reaction/1173165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl 2,7-diazaspiro[3.5]nonane-2-carboxylateHCID 23282935—
Reactanttert-Butyl 2-(6-chloronicotinamido)-4-(thiophen-2-yl)phenylcarbamateHCID 57717453—
SolventDimethyl SulfoxideHCID 679—
ProductN-[2-amino-5-(2-thienyl)phenyl]-6-(2,7-diazaspiro[3.5]non-7-yl)nicotinamideHCID 52916957—

Reaction Conditions

Temperature90 °C

Reaction Steps

tert-Butyl[2-{[(6-chloropyridin-3-yl)carbonyl]amino}-4-(2-thienyl)phenyl]carbamate F (20 mg, 0.088 mmol) was dissolved in 1 mL of DMSO and treated with Et3N(0.010 mL) and tert-butyl 2,7-diazaspiro[3.5]nonane-2-carboxylate (20 mg, 0.047 mmol). The mixture was stirred at 90° C. for 18 h, partitioned between EtOAc and saturated NaHCO3, dried (MgSO4), filtered and concentrated), concentrated and the residue was purified by chromatography on SiO2 (EtOAc/CH2Cl2, 0% to 100%). The residue was dissolved in 1 mL of 1:1 TFA/CH2Cl2, stirred for 1 h and concentrated. Neutralization with EtOAc/sat'd NaHCO3 extraction and drying (MgSO4) gave desired product, N-[2-amino-5-(2-thienyl)phenyl]-6-(2,7-diazaspiro[3.5]non-7-yl)nicotinamide, which was confirmed by MS (ESI+): cal'd [M+H]+ 420.2, obs'd 420.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834026B2
Source datasetuspto-grants-2010_11
ORD IDord-bb776e9005d84d6a9e3bb0270804560b
Source noteuspto-grants-2010_11