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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634081Generated: November 2, 2026

Ethyl Acetate → 5-(Aminomethyl)-1-(2-tetrahydropyranyl)indazole

https://huagongshe.com/reaction/1634081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
Reactant5-(Azidomethyl)-1-(2-tetrahydropyranyl)indazoleHCID 10539077—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product5-(Aminomethyl)-1-(2-tetrahydropyranyl)indazoleHCID 1082341892%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of LiAlH4 (Aldrich, 10.5 mL, 10.5 mmol, 1.0 M) in THF was added dropwise into a yellow solution of 5-(azidomethyl)-1-(2-tetrahydropyranyl)indazole (compound 109, 2.6 g, 10.1 mmol) in THF (30 mL) at 0° C. After stirring at 0° C. for 1 hour, NaOH (1.0M, 1.5 mL) was added. The reaction mixture was allowed to warm to room temperature. Ethyl acetate (100 mL) was added, and the suspension was filtered (Celite). The filter cake was washed with an addition portion of ethyl acetate (40 mL). Combined organic layers were evaporated under vacuum to give free amine 110 (2.14 g, 92%). MS (electrospray) 232.5 (M+1); 1H NMR (CDCl3) δ 1.61 (m, 3H), 2.02 (m, 2H), 2.50 (m, 1H), 2.83 (br s, 2H), 3.68 (m, 1H), 3.85 (s, 2H), 3.95 (m, 1H), 5.62 (d, 1H, J=9.2 Hz), 7.29 (d, 1H, J=8.8 Hz), 7.48 (d, 1H, J=8.8 Hz), 7.53 (s, 1H), 7.92 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506754B1
Source datasetuspto-grants-2003_01
ORD IDord-11a814eb98ec438abb2b02145119eae9
Source noteuspto-grants-2003_01