Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890517Generated: November 1, 2026

Triethylamine → N-Methoxy-N-methylthieno[3,2-c]pyridine-2-carboxamide

https://huagongshe.com/reaction/1890517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantThieno[3,2-c]pyridine-2-carboxylic acidHCID 13580293—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-Methoxy-N-methylthieno[3,2-c]pyridine-2-carboxamideHCID 86671431—

Reaction Steps

To a solution of thieno[3,2-c]pyridine-2-carboxylic acid (D′-1) (11.5 g, 64.2 mmol) in DCM (200 mL) and DMF (50 mL) was added Et3N (19.5 g, 26.6 mL, 192.6 mmol) followed by HATU (36.6 g, 96.3 mmol). The reaction solution was stirred at room temperature for 20 mins, and then treated with N,O-dimethylhydroxylamine hydrochloride (6.9 g, 70.6 mmol). Stirring continued overnight at room temperature. The solvent was removed. The residue was dissolved in EtOAc and washed with water and brine. The organic layer was dried and concentrated. The residue was purified by chromatography on silica gel to give the title compound. MS (m/z): 223 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507487B2
Source datasetuspto-grants-2013_08
ORD IDord-e6c45ab05544423b939eb2dd8c7d8675
Source noteuspto-grants-2013_08