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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825712Generated: November 3, 2026

Pyridine → HCID 21868813, compound

https://huagongshe.com/reaction/1825712

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 (VII)(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. 1H NMR (300 MHz, CDCl3) δ 12.18 (s, 1H), 8.88 (d, J=8.9 Hz, 1H), 7.82 (dd, J=1.9, 8.9 Hz, 1H), 7.71 (d, J=1.9 Hz, 1H), 7.51 (dd, J=2.6, 8.9 Hz, 1H), 7.41 (d, J=2.6 Hz, 1H), 6.97 (d, J=8.9 Hz, 1H), 4.08 (s, 2H), 3.70 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049309B2
Source datasetuspto-grants-2006_05
ORD IDord-cf267ab6d27a46a183a4e1890a517d7d
Source noteuspto-grants-2006_05