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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77100Generated: October 29, 2026

tert-Butyl piperazine-1-carboxylate → HCID 178423455, compound

https://huagongshe.com/reaction/77100

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 178423460HCID 178423460—
SolventDichloromethaneHCID 6344—
ProductHCID 178423455HCID 17842345515%

Reaction Conditions

Temperature35 °C

Reaction Steps

Method I—Step a To a vial with [1-[4-Fluoro-3-(5-methyl-1H-benzoimidazol-2-yl)-phenyl]-piperidine-4-carboxylic acid hydrochloride (obtained as described in general method 8, step b) (0.10 g, 0.26 mmol) and HATU (0.10 g, 0.27 mmol) in dichloromethane (2 mL), TEA (0.08 mL, 0.56 mmol) and tert-butyl-1-piperazinecarboxylate (0.32 mmol, 0.06 g) were added. The reaction mixture was heated at 35° C. overnight, washed with water (3×2 mL) and saturated Na2CO3 solution (3×2 mL). The crude was then purified by flash chromatography (eluent: EtOAc), and then a filtration on an NH2 cartridge was run (eluent EtOAc), to obtain 0.02 g of the title compound (15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835648B2
Source datasetuspto-grants-2014_09
ORD IDord-e3874e82526544a18e548bf20ff15cab
Source noteuspto-grants-2014_09