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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857439Generated: October 28, 2026

Pyridine → HCID 21868813, compound

https://huagongshe.com/reaction/857439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBromoacetyl bromideHCID 61147—
ReactantHCID 10947474HCID 10947474—
SolventDichloromethaneHCID 6344—
ProductHCID 21868813HCID 21868813—

Reaction Steps

To a solution of (2-Amino-5-trifluoromethyl-phenyl)-(5-chloro-2-methoxy-phenyl)-methanone (IV) (14.13 g, 42.9 mmol, 1 eq) in Dichloromethane (120 mL) at 0° C. was added pyridine (4.65 mL, 57.5 mmol, 1.34 eq), then Bromoacetyl bromide (4.98 mL, 57.2 mmol, 1.33 eq). After 3 h, the reaction was quenched with Sodium bicarbonate (aq) and extracted three times into Dichloromethane. The combined organic layers were dried over Magnesium sulfate, filtered and concentrated in vacuo. The product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07145013B2
Source datasetuspto-grants-2006_12
ORD IDord-aad0ed3b21fb4184b7e1fbf416294eec
Source noteuspto-grants-2006_12