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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360551Generated: November 3, 2026

Triethylamine → 8-[5-({[2-Amino-5-(2-thienyl)phenyl]amino}carbonyl)pyridin-2-yl]-N-ethyl-1,8-diazaspiro[4.5]decane-1-carboxamide

https://huagongshe.com/reaction/2360551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactantn-Ethyl-1,8-diazaspiro[4.5]decane-1-carboxamideHCID 57717467—
ReactantButyl[2-{[(6-Chloropyridin-3-yl)carbonyl]amino}-4-(2-thienyl)phenyl]-carbamateHCID 86685290—
SolventDimethyl SulfoxideHCID 679—
Product8-[5-({[2-Amino-5-(2-thienyl)phenyl]amino}carbonyl)pyridin-2-yl]-N-ethyl-1,8-diazaspiro[4.5]decane-1-carboxamideHCID 24745117—

Reaction Steps

A solution of intermediate F (82 mg, 0.19 mmol), N-ethyl-1,8-diazaspiro[4.5]-decane-1-carboxamide (73 mg, 0.35 mmol), and NEt3 (43 μL, 0.31 mmol) in 5 mL of DMSO was stirred at 90° C. for 12 h. The reaction mixture was partitioned between EtOAc and saturated NaHCO3, the organic layer was dried (MgSO4), filtered and concentrated. The residue was stirred in 2 mL of TFA and 2 mL of CH2Cl2 for 1 h at room temperature and concentrated. Reverse-phase chromatography (10 to 100% MeCN/water with 0.05% TFA) followed by neutralization with EtOAc/saturated NaHCO3 extraction and drying with MgSO4 gave the title compound: MS (ESI+): cal'd [M+H]+ 505.2, obs'd 505.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686020B2
Source datasetuspto-grants-2014_04
ORD IDord-6d4c41c8e2704c538ca71081f0ffcb0d
Source noteuspto-grants-2014_04