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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72801Generated: October 29, 2026

Sodium t-butoxide → 2-Pyrrolidin-1-yl-4-p-tolyl-7,8-dihydro-5H-pyrido[4,3-d]pyrimidine-6-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/72801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium t-butoxideHCID 23676156—
ReactantPyrrolidine-1-carboxamidine trifluoroacetateHCID 67370060—
Reactant3-(4-Methyl-benzoyl)-4-oxo-piperidine-1-carboxylic acid tert-butyl esterHCID 67372332—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product2-Pyrrolidin-1-yl-4-p-tolyl-7,8-dihydro-5H-pyrido[4,3-d]pyrimidine-6-carboxylic acid tert-butyl esterHCID 6736981036.7%

Reaction Steps

To a mixture of 3-(4-Methyl-benzoyl)-4-oxo-piperidine-1-carboxylic acid tert-butyl ester (0.24 g, 0.74 mmol) and pyrrolidine-1-carboxamidine trifluoroacetate (0.14 g, 0.58 mmol) in t-BuOH (7.5 mL) was added sodium tert-butoxide (0.10 g, 1.1 mmol). The mixture was heated at reflux for 2 h, then cooled to rt, diluted with H2O and extracted with CH2Cl2 (2×). The combined organic extracts were dried and concentrated. The residue was purified by FCC to give the title compound (0.084 g, 29%) as a clear oil. MS (ESI): mass calcd. for C23H30N4O2, 394.5; m/z found, 395.5 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829011B2
Source datasetuspto-grants-2014_09
ORD IDord-805c9fc3f1c040e096cbd139ab11fe2e
Source noteuspto-grants-2014_09