Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284891Generated: October 30, 2026

tert-Butanol → HCID 86729618, compound

https://huagongshe.com/reaction/2284891

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
Reactanttert-butyl (3S)-3-aminopiperidine-1-carboxylateHCID 1501975—
Reactant2,4-Dichloro-5-(trifluoromethyl)pyrimidineHCID 2782774—
CatalystZincchlorideHCID 3007855—
Solvent1,1-DichloroethaneHCID 6365—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 86729618HCID 8672961857.1%

Reaction Steps

To a solution of 2,4-dichloro-5-(trifluoromethyl)pyrimidine (5 g, 23 mmol) in dichloroethane: t-butanol (50 ml, 1:1) was added dry zinc chloride (3.7 g, 27 mmol) and triethylamine (2.52 g, 25 mmol), and the mixture was stirred at rt for 1 h (pH should not be >7). To this mixture, (S)-tert-butyl 3-aminopiperidine-1-carboxylate (4.9 g, 25 mmol) was added and stirring continued at rt for 16 h. TLC showed formation of the major compound (0.2 Rf) and a minor other isomer (0.25 Rf) and ˜10% starting material in 15% EtOAc: hexane solvent system. Solvents were evaporated, and crude was diluted with ice cold water (50 mL) and stirred for 5 min at rt to get a pale yellow gummy mass. The crude pale yellow gummy mass (6 g) was taken in 60 mL hexane and stirred for 10 min at rt to get a solid which was immediately filtered to get the pure desired compound (5 g, 57%). MS m/z: 381.1 (ES+, M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145387B2
Source datasetuspto-grants-2015_09
ORD IDord-7feac5b84b0645f2b23f8d7dd8582168
Source noteuspto-grants-2015_09