Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354230Generated: November 2, 2026

Triethylamine → HCID 86603235, compound

https://huagongshe.com/reaction/1354230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium AzideHCID 33557—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 69520111HCID 69520111—
SolventDichloromethaneHCID 6344—
ProductHCID 86603235HCID 86603235—

Reaction Conditions

Temperature80 °C

Reaction Steps

At 0° C., triethylamine (3.7 ml, 26.2 mmol) and, dropwise, methanesulphonyl chloride (1.2 ml, 15.44 mmol) were added to a solution of tert-butyl 5-hydroxymethyl-3,6-dihydro-2H-pyridine-1-carbamate (Tetrahedron 1998, 54, 7045–7056, 2.8 g, 13.1 mmol) in DCM (50 ml). The reaction mixture was stirred at 0° C. for 20 minutes before a saturated solution of NaHCO3 (40 ml) was added, and the two phases were separated. The aqueous phase was extracted with dichloromethane (40 ml). The combined organic phases were washed with saturated sodium chloride solution and dried over MgSO4 and concentrated. The crude product was dissolved in DMF (50 ml), and sodium azide (1.7 g, 26.1 mmol) was added. The mixture was heated to 80° C. Reaction monitored by LCMS. Once the reaction was complete, the mixture was cooled and concentrated. The residue was taken up in EtOAc and water and the aqueous phase was extracted with EtOAc (2×100 ml). The combined organic phases were washed with saturated sodium chloride solution, dried over MgSO4 and concentrated. The residue was purified by chromatography on silica gel (EtOAc/hex 1/6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223776B2
Source datasetuspto-grants-2007_05
ORD IDord-1802a08561534e0e911374d1b8f5c63a
Source noteuspto-grants-2007_05