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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634074Generated: October 30, 2026

Ethyl Acetate → 1h-Indazole-6-methanamine,1-(tetrahydro-2h-pyran-2-yl)-

https://huagongshe.com/reaction/1634074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
Reactant6-(Azidomethyl)-1-(2-tetrahydropyranyl)indazoleHCID 18616189—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product1h-Indazole-6-methanamine,1-(tetrahydro-2h-pyran-2-yl)-HCID 18616200—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of LiAlH4 (9 mL, 9 mmol, 1.0 M) in THF was added dropwise to a yellow solution of 6-(azidomethyl)-1-(2-tetrahydropyranyl)indazole (2.4 g, 9 mmol) (8) in THF (30 mL) at 0° C. After stirring at 0° C. for 1 hour, NaOH (1.0 m, 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 through (Celite). The filter cake was washed with an addition portion of ethyl acetate (40 mL). Combined organic layers were evaporated under vacuum to five essentially pure amine (2.1 g, 97%). MS (electrospray) 232.5 (M+1); 1H NMR (CDCl3) δ 1.67 (m, 3H), 2.01 (m, 2H), 2.48 (m, 1H), 3.85 (m, 1H), 3.94 (m, 1H), 5.75 (d, 1H, J=9.4 Hz), 7.14 (d, 1H, J=8.4 Hz), 7.62 (s, 1H), 7.62 (d, 1H, J=8.4 Hz), 7.93 (s, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506754B1
Source datasetuspto-grants-2003_01
ORD IDord-09e8816e570e4c848baa345c11c6d947
Source noteuspto-grants-2003_01