Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131115Generated: November 1, 2026

Phosphoric Acid → 4-(2-Chloro-pyrido[2,3-d]pyrimidin-4-yl)-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/131115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
Reactant2-Aminonicotinic acidHCID 72930—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant2,4-Dichloro-pyrido[2,3-d]pyrimidineHCID 22222228—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
Product4-(2-Chloro-pyrido[2,3-d]pyrimidin-4-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 5973212740%

Reaction Steps

A mixture of 2,4-dichloro-pyrido[2,3-d]pyrimidine (150 mg, 0.75 mmol, 1 eq) [prepared from 2-aminonicotinic acid by the methods of Robins et al. (J. Am. Chem. Soc. 1955, 77, 1045.) and Oakes et al. (J. Chem. Soc. 1956, 1045.)], N-t-butoxycarbonyl piperazine (147 mg, 0.787 mmol, 1.05 eq) and Hunig's base (0.39 mL, 2.25 mmol, 3 eq) in ethanol (2.5 mL) was stirred at rt for 17 hr. The white solid was collected by filtration, washed with water and cold ethanol, and dried to afford C1.1 (105 mg, 40% yield). LC/MS: 350.41 [M+H]+; HPLC: >95% at 1.44 min (Xterra 5 μm C18 column 4.6×30 mm, 10-90% aqueous methanol over 2 min containing 0.2% phosphoric acid, 5 mL/min, monitoring at 254 nm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384937B2
Source datasetuspto-grants-2008_06
ORD IDord-467352c9ade34758b898e0f93e8468b3
Source noteuspto-grants-2008_06