Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427666Generated: October 25, 2026

Phosgene → 5-(tert-butyldimethylsilyloxy)-2-phthalimido-N-[[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl]aniline

https://huagongshe.com/reaction/427666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
Reactant(1-(Pyridin-4-YL)piperidin-4-YL)methanolHCID 11310048—
Reactant5-(Tert-butyldimethylsilyloxy)-2-phthalimidoanilineHCID 18174494—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Product5-(tert-butyldimethylsilyloxy)-2-phthalimido-N-[[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl]anilineHCID 1817452990%

Reaction Steps

A solution of 5-(tert-butyldimethylsilyloxy)-2-phthalimidoaniline (1.02 g, 2.77 mmol) in toluene (15 mL) was treated with a solution of 20% phosgene in toluene (2 mL) at reflux for 20 min. The volatile materials were removed in vacuo to give a tan solid, which was dissolved in dry methylene chloride (20 mL) and treated with 1-(4-pyridyl)piperidine-4-methanol (0.53 g, 2.77 mmol). The resulting suspension was stirred for 90 min then diluted with hexane. The mixture was allowed to stand overnight and the resulting precipitate collected by vacuum filtration and dried to yield 1.46g (90%) of the title compound as a tan powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313122B1
Source datasetuspto-grants-2001_11
ORD IDord-3a0241fc12ef445383c48e33e9ce0cda
Source noteuspto-grants-2001_11