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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712008Generated: October 29, 2026

Triethylamine → N-[(2S)-Bicyclo[2.2.1]hept-2-yl]-6-nitrothieno[3,2-b]pyridin-7-amine

https://huagongshe.com/reaction/712008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantExo-2-bornanamineHCID 98480—
Reactant7-Chloro-6-nitrothieno[3,2-b]pyridineHCID 14207950—
SolventIsopropanolHCID 3776—
ProductN-[(2S)-Bicyclo[2.2.1]hept-2-yl]-6-nitrothieno[3,2-b]pyridin-7-amineHCID 86717467—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 7-chloro-6-nitrothieno[3,2-b]pyridine (0.064 g, 0.30 mmol) (Example 1, Step 2), bicyclo[2.2.1]heptan-2-amine (from Aldrich, 0.050 g, 0.45 mmol) and triethylamine (0.083 mL, 0.60 mmol) in isopropyl alcohol (1.4 mL) was heated at 90° C. for 2 h. The mixture was concentrated to give the desired product, which was used in the next step without further purification. LCMS calculated for C14H16N3O2S (M+H)+: m/z=290.1. Found: 290.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181271B2
Source datasetuspto-grants-2015_11
ORD IDord-54ef6981dadd4cf3a965b36f16d96355
Source noteuspto-grants-2015_11