Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867182Generated: October 30, 2026

Isopropyl chloroformate → N-[5,8-dihydro-2-(4-formyl-1-piperazinyl)-5-oxopyrido[2,3-d]pyrimidine-6-carbonyloxy]succinimide

https://huagongshe.com/reaction/867182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl chloroformateHCID 7917—
ReactantTriethylamineHCID 8471—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant5,8-Dihydro-2-(4-formyl-1-piperazinyl)-5-oxopyrido[2,3-d]pyrimidine-6-carboxylic acidHCID 12850757—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-[5,8-dihydro-2-(4-formyl-1-piperazinyl)-5-oxopyrido[2,3-d]pyrimidine-6-carbonyloxy]succinimideHCID 1286637290.5%

Reaction Steps

A suspension of 5,8-dihydro-2-(4-formyl-1-piperazinyl)-5-oxopyrido[2,3-d]pyrimidine-6-carboxylic acid (273 g) and triethylamine (299 ml) in dried dichloromethane (3500 ml) was stirred well at room temperature for one hour. To the suspension, isopropyl chloroformate (221 g) was added dropwise with cooling at 0°-10° C. and the reaction mixture was stirred for 2 hours. A solution of N-hydroxysuccinimide (207 g) in dimethylformamide (350 ml) was added to the mixture and the resulting mixture was kept at 5°-10° C. for additional 2 hours. The crystalline product was collected by filtration and washed successively with water (2000 ml) and acetone (2000 ml) to give N-[5,8-dihydro-2-(4-formyl-1-piperazinyl)-5-oxopyrido[2,3-d]pyrimidine-6-carbonyloxy] succinimide (326 g). m.p. above 300° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04103011
Source datasetuspto-grants-1978_07
ORD IDord-d76ea2ae5e8e4b36aa4ffde92fd9b171
Source noteuspto-grants-1978_07