Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325081Generated: October 30, 2026

Sodium Hydroxide → 3,4,5,6,7,8-Hexahydro-3-[2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl]pyrido[4',3'; 4,5]thieno[2,3-d]pyrimidin-4-one

https://huagongshe.com/reaction/325081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3,4,5,6,7,8-Hexahydro-7-acetyl-3-[2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl]pyrido[4',3':4,5]thieno[2,3-d]pyrimidin-4-oneHCID 9804624—
SolventHydrochloric AcidHCID 313—
Product3,4,5,6,7,8-Hexahydro-3-[2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl]pyrido[4',3'; 4,5]thieno[2,3-d]pyrimidin-4-oneHCID 988865766%

Reaction Conditions

Temperature100 °C

Reaction Steps

4.0 g (8.6 mmol) of 3,4,5,6,7,8-hexahydro-7-acetyl-3-[2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl]pyrido[4′,3′:4,5]thieno[2,3-d]pyrimidin-4-one were dissolved in 80 ml of 10% strength hydrochloric acid and stirred at a bath temperature of 100° C. for 2 h. The mixture was then poured into ice-water, made alkaline with concentrated sodium hydroxide solution and extracted twice with methylene chloride. The combined organic phases were dried and concentrated. 3.7 g of crude product were isolated and were recrystallized from 50 ml of isopropanol. 2.4 g (66%) of product with melting point 168-170° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06222034B1
Source datasetuspto-grants-2001_04
ORD IDord-97d180a953214980a616361d4140656c
Source noteuspto-grants-2001_04