Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299306Generated: October 25, 2026

N-(4-chlorobenzyl)-7-methyl-2-(4-morpholinylmethyl)-4-oxo-4,7-dihydrothieno(2,3-b)pyridine-5-carboxamide → Thieno(2,3-b)pyridine-5-carboxamide, N-((4-chlorophenyl)methyl)-4,7-dihydro-7-methyl-2-(4-morpholinylmethyl)-4-oxo-, hydrochloride (1:1)

https://huagongshe.com/reaction/2299306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-chlorobenzyl)-7-methyl-2-(4-morpholinylmethyl)-4-oxo-4,7-dihydrothieno(2,3-b)pyridine-5-carboxamideHCID 503580—
SolventHydrochloric AcidHCID 313—
ProductThieno(2,3-b)pyridine-5-carboxamide, N-((4-chlorophenyl)methyl)-4,7-dihydro-7-methyl-2-(4-morpholinylmethyl)-4-oxo-, hydrochloride (1:1)HCID 18380160179.3%

Reaction Steps

N-(4-chlorobenzyl)-7-methyl-2-(4-morpholinylmethyl)-4-oxo-4,7-dihydro-thieno[2,3-b]pyridine-5-carboxamide (1.50 g) from Example No. 36 is dissolved in methanolic HCl (50 mL) and concentrated in vacuo. The resulting off-white solid is recrystallized from methanol/ethanol to yield 1.458 g (90%) of the title compound as a white solid. Physical characteristics are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495683B2
Source datasetuspto-grants-2002_12
ORD IDord-df221610b9cd49ada947e9d0dbd21160
Source noteuspto-grants-2002_12