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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263441Generated: October 30, 2026

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

https://huagongshe.com/reaction/1263441

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) (101) in THF (30 mL) at 0° C. The addition time was 10 minutes, and gas came out. 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) δ1.67 (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 numberUS06541467B1
Source datasetuspto-grants-2003_04
ORD IDord-82ec485aaffa4b7db2bf75d48e872290
Source noteuspto-grants-2003_04