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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634178Generated: October 30, 2026

Water → 5-(Azidomethyl)-1-(2-tetrahydropyranyl)indazole

https://huagongshe.com/reaction/1634178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium AzideHCID 33557—
Reactant5-(Bromomethyl)-1-(2-tetrahydropyranyl)indazoleHCID 10565781—
SolventDimethylformamideHCID 6228—
Product5-(Azidomethyl)-1-(2-tetrahydropyranyl)indazoleHCID 1053907799.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 5-(bromomethyl)-1-(2-tetrahydropyranyl)indazole (compound 12-5, 3.0 g, 10.2 mmol) in DMF (30 mL), was added with sodium azide (Aldrich, 2.64 g, 40.6 mmol) in one portion. The suspension was heated at 90° C. for 30 minutes and a yellow solution was formed. After cooling to room temperature, the reaction mixture was poured into water (100 mL) and extracted with ether (2×150 mL). Combined organic layers were washed with brine, then dried (MgSO4). Evaporation of solvent gave the product (12-6) as a yellow oil (2.61 g, 99%). TLC Rf 0.63 (60:40 hexane-ethyl acetate); MS (electrospray) 258 (M+1); 1H NMR (CDCl3) δ2.03-2.15 (m, 2H), 2.55 (m, 1H), 3.72 (m, 1H), 4.02 (m, 1H), 4.52 (s, 1H), 5.71 (d, 1H, J=9.4 Hz), 7.32 (d, 1H, J=8.8 Hz), 7.56 (d, 1H, J=8.8 Hz), 7.63 (s, 1H), 8.00 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506761B1
Source datasetuspto-grants-2003_01
ORD IDord-cb45f07c5ddb4695960958e3b2d70c5c
Source noteuspto-grants-2003_01