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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385086Generated: November 1, 2026

Water → 1-Cyclopentyl-3-ethyl-1H-indazole-6-carboxylic Acid Methyl Ester

https://huagongshe.com/reaction/1385086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBromocyclopentaneHCID 8728—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178438014HCID 178438014—
SolventDimethylformamideHCID 6228—
Product1-Cyclopentyl-3-ethyl-1H-indazole-6-carboxylic Acid Methyl EsterHCID 1589608272.1%

Reaction Steps

1.17 g (29.4 mmol, 1.05 equiv) sodium hydride, 60% oil dispersion, were added in one portion to a room temperature solution of 5.7 g (27.9 mmol, 1.0 equiv) 3-ethyl-1H-indazole-6-carboxylic acid methyl ester in 125 mL anhydrous DMF. After 20 minutes, 3.89 mL (36.6 mmol, 1.3 equiv) cyclopentyl bromide were added dropwise, and the reaction mixture allowed to stir overnight at room temperature. The mixture was then poured into 1 L H2O and extracted 3×400 mL H2O, 1×200 mL brine, and dried over Na2SO4. Filtration, concentration of filtrate and drying gave an amber oil, which was purified on a silica gel column (10% ethyl acetate/hexanes, gravity) to give 5.48 g (72%) of a clear oil: 1H MR (300 MHz, CDCl3) δ 8.16 (d, 1H, J=1.0 Hz), 7.7 (m, 2H), 500 (quintet, 1H, J=7.5 Hz), 3.97 (s, 3H), 3.01 (q, 2H, J=7.6 Hz), 2.2 (m, 4H), 2.0 (m, 2H), 1.8 (m, 2H), 1.39 (t, 3H, J=7.6 Hz); HRMS calc for C16H20N2O2: 272.1526. Found: 272.15078.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262040B1
Source datasetuspto-grants-2001_07
ORD IDord-89e89fcedb14494d91ce36aeac3510f3
Source noteuspto-grants-2001_07