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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935458Generated: October 30, 2026

Acetic Anhydride → Ethyl n-(3-carboethoxy-6-methyl-4,5,6,7-tetrahydrothieno-[2,3-c]pyridin-2-yl)ethaneimidate

https://huagongshe.com/reaction/1935458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethyl orthoacetateHCID 66221—
ReactantThieno(2,3-c)pyridine-3-carboxylic acid, 4,5,6,7-tetrahydro-2-amino-, ethyl ester,HCID 212359—
ProductEthyl n-(3-carboethoxy-6-methyl-4,5,6,7-tetrahydrothieno-[2,3-c]pyridin-2-yl)ethaneimidateHCID 5422734893%

Reaction Steps

0.8 ml of acetic anhydride was added to 3.0 g (12.5 mmol) of 2-amino-3-carboethoxy-4,5,6,7-tetrahydrothieno[2,3-c]pyridine in 25 ml of triethyl orthoacetate and the mixture was boiled under nitrogen and at reflux for 2 h. After that, the mixture was evaporated right down at 80° C. on a rotary evaporator. 3.6 g (93%) of crude product were isolated as a dark oil, which is sufficiently pure for further reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06387912B1
Source datasetuspto-grants-2002_05
ORD IDord-040096e4e7ab4db5a3658d54109acac4
Source noteuspto-grants-2002_05