Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713716Generated: October 30, 2026

Triethylamine hydrochloride → HCID 178452323, compound

https://huagongshe.com/reaction/713716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamine hydrochlorideHCID 11130—
ReactantSodium AzideHCID 33557—
ReactantTert-butyl 4-(cyanomethyl)piperazine-1-carboxylateHCID 21936030—
SolventTolueneHCID 1140—
ProductHCID 178452323HCID 17845232363%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred suspension of 1.50 g (6.66 mmol) of the title compound from Step A above in 25 mL of anhydrous toluene was added 1.38 g (10.0 mol) of triethylamine hydrochloride followed by 0.65 g (10 mmol) of sodium azide. The resulting mixture was heated to 80° C. for 12 h then cooled to ambient temperature. All volatiles were removed in vacuo, and the residue suspended in 5 mL of brine and 1.0 N aqueous hydrogen chloride solution was added until pH of ˜4 was achieved. The aqueous phase was extracted with chloroform and the combined organics were dried over magnesium sulfate and evaporated to dryness in vacuo. The residue was purified by silica gel chromatography eluting with a 0-100% acetone in hexanes gradient to afford the title compound (i-18) as white solid (1.1 g, 63%). 1H-NMR (500 MHz, DMSO-d) δ 3.82 (s, 2H), 3.29 (br s, 4H), 2.38-2.34 (m, 4H), 1.36 (s, 9H). LC-MS: m/z (ES) 269.0 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09186354B2
Source datasetuspto-grants-2015_11
ORD IDord-4bc4ae2f2bb9406ba7feab0f37ae1784
Source noteuspto-grants-2015_11