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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713433Generated: October 30, 2026

Ethyl bromoacetate → HCID 178472607, compound

https://huagongshe.com/reaction/713433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantTriethylamineHCID 8471—
ReactantHCID 178505426HCID 178505426—
ProductHCID 178472607HCID 17847260733.3%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a suspension of ethyl 2-bromoacetate (0.55 g, 3.3 mmol) and 6-fluoro-3-piperidin-4-yl-1H-indazole (0.60 g, 2.7 mmol in 10 mL of acetonitrile) was added Et3N (1.4 g, 13.7 mmol) and the reaction mixture was stirred at 85° C. for 15 hours. The reaction mixture was cooled to ambient temperature and the solvent was removed in vacuo. The residue was redissolved in DCM (50 mL), washed with water, brine, dried over Na2SO4 and concentrated in vacuo. Purification by flash chromatography gave the title compound (0.29 g, 0.90 mmol) as a white solid. MS (ESI) m/z 306.9 (M+H+); HPLC (Novapak 150×3.9 mm C-18 column: mobile phase: 35-90% acetonitrile/water with 0.1% TFA, at 2 mL/min over 2 min.) t 1.54 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181266B2
Source datasetuspto-grants-2015_11
ORD IDord-85658d98313c4d19a2e465b44e7bd8c3
Source noteuspto-grants-2015_11