Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23002Generated: October 25, 2026

Water → 3-Methoxypropyl indazole amide

https://huagongshe.com/reaction/23002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1-Bromo-3-methoxypropaneHCID 524551—
Reactant1H-Indazole-3-carboxamideHCID 20978176—
SolventDimethylformamideHCID 6228—
Product3-Methoxypropyl indazole amideHCID 86587456—

Reaction Conditions

Temperature60 °C

Reaction Steps

Following the procedure for converting Compound 1e to Compound 1f, the indazole amide Compound 1e (0.31 g, 17.8 mmol) was treated with 1-bromo-3-methoxypropane (0.3 g, 19.6 mmol) in the presence of 95% NaH (0.05 g, 19.6 mmol) in DMF (50 mL) at 0° C. for 20 min and then warmed to 60° C. for 2 h. The mixture was cooled down to rt. Water was added and the aqueous solution was extracted with EtOAc several times. The organic layers were combined and washed with brine, then dried (Na2SO4) and evaporated in vacuo to an oil. The oil was purified by flash column chromatography (96:4:0.4; DCM:MeOH:NH4OH) to afford a 3-methoxypropyl indazole amide analog of Compound 1f (0.32 g, 73%). 1H NMR (CDCl3) δ 7.69 (d, J=8.13 Hz, 1H), 7.4 (m, 2H), 7.17 (m, 1H), 6.57 (bd s, 1H), 5.39 (bd s, 1H), 4.47 (t, J=6.65 Hz, 2H), 3.96 (s, 2H), 3.30 (t, J=5.78 Hz, 2H), 3.28 (s, 3H), 2.16 (m, 2H). ES-MS m/z 248 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849643B2
Source datasetuspto-grants-2005_02
ORD IDord-13736acf64db4915ace7a9a9b5695486
Source noteuspto-grants-2005_02