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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464138Generated: October 31, 2026

Ethanol → 4-(2-[2-amino-4,5,6,7-tetrahydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-5-yl]ethyl)benzoic acid

https://huagongshe.com/reaction/1464138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantGuanidine HydrochlorideHCID 5742—
ReactantSodium hydrideHCID 24758—
ReactantSodium ethoxideHCID 2723922—
Reactant4-(2-(2-Thiocarbonyl-3-carboethoxypyrrolidin-4-yl)ethyl)benzoic acidHCID 20097521—
Product4-(2-[2-amino-4,5,6,7-tetrahydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-5-yl]ethyl)benzoic acidHCID 13551274680.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of sodium ethoxide in ethanol [prepared by reaction of 1.06 grams (44.1 mmol) of sodium hydride and 50 ml of ethanol] was combined with 4.22 grams (44.1 mmol) of guanidine HCl and then stirred at 50° C. for 20 minutes. The cooled suspension was filtered (celite) to remove NaCl and the filtrate was mixed with 2.83 grams (8.81 mmol) of 4-(2-(2-thiocarbonyl-3-carboethoxypyrrolidin-4-yl)ethyl)benzoic acid. The resulting solution was concentrated in vacuo to remove most of the alcohol and the residue was slowly heated to 90° C. while maintaining a vacuum of 10 torr. After heating 1 additional hour, the mixture was cooled and the reaction product taken up in 75 ml of water. The pH of the mixture was adjusted to 6 by addition of 6M HCl and the mixture was then filtered. The precipitate was consecutively washed with 20 ml water, 20 ml methanol, and 40 ml ether. After drying, 2.13 grams (64%) of 4-(2-[2-amino-4,5,6,7-tetrahydro-4-oxo-3H-pyrrolo[2,3-d]pyrimidin-5yl]ethyl)benzoic acid was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05302722
Source datasetuspto-grants-1994_04
ORD IDord-eb0fbf6763b3438482d5a30d1f3e80ff
Source noteuspto-grants-1994_04