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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589398Generated: October 29, 2026

Triethylamine → ethyl 2-[1-[4-(6-methylnicotinamido)benzyl]-1H-indazol-3-yl]acetate

https://huagongshe.com/reaction/589398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Methylnicotinoyl chlorideHCID 21890458—
Reactantethyl 2-[1-(4-aminobenzyl)-1H-indazol-3-yl]acetateHCID 89590263—
SolventDichloromethaneHCID 6344—
Productethyl 2-[1-[4-(6-methylnicotinamido)benzyl]-1H-indazol-3-yl]acetateHCID 8959026472.5%

Reaction Steps

Ethyl 2-[1-(4-aminobenzyl)-1H-indazol-3-yl]acetate (258 mg, 0.83 mmol) and triethylamine (0.4 mL, 2.87 mmol) were dissolved in dichloromethane (15 mL), and in an ice bath, dichloromethane solution (10 mL) of the prepared 6-methylnicotinoyl chloride (about 1.00 mmol) was added dropwise slowly. Upon completion of the dropwise addition, it was reacted at room temperature for 16 hours. An aqueous solution of sodium bicarbonate was added to quench, and extracted with ethyl acetate. The organic phase was dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduce pressure, and chromatographed on a silica gel column (petroleum ether:ethyl acetate=2:1) to obtain a white solid 258 mg, at a yield of 72.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233098B2
Source datasetuspto-grants-2016_01
ORD IDord-5666e46ff67c4423bf9b6c10c3acbb4c
Source noteuspto-grants-2016_01