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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684104Generated: November 1, 2026

Pyridine → HCID 10052502, compound

https://huagongshe.com/reaction/1684104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDimethylformamideHCID 6228—
ReactantBromoacetyl chlorideHCID 89602—
ReactantPotassium BromideHCID 253877—
ReactantHCID 9970997HCID 9970997—
SolventButanol acetic acid waterHCID 22056973—
ProductHCID 10052502HCID 10052502—

Reaction Steps

To a solution of 503 mg (1.42 mmol) of 9 .2HCl in 15 mL of dry dimethyl formamide were added sequentially, 533 μL (6.59 mmol) of pyridine and 282 μL (3.42 mmol) of bromoacetyl chloride. After allowing the mixture to stir at room temperature for 6 hours, the precipitated product was filtered off and rinsed with water and then rinsed with ethanol: 393 mg (53%) yield; mp 308°-310° C.; TLC (n-butanol/acetic acid/water [5:2:3]), Rf =0.58; IR (KBr pellet) 3380, 3278, 1681, 1638, 1551, 1472, 1411, 1325, 1238, 1047 cm-1 ; 1H NMR (dimethyl-d6 sulfoxide) δ9.72 (2H, s, 2- and 5-acetamido N(H), 7.87 (2H, brs, 3- and 6-carbamyl proton), 4.22 (4H, s, methylenes), 3.65 (6H, s, methoxys), 2.70 (6H, d, J=4.6 Hz, 3- and 6-carbamyl methyl); mass spectrum (EI mode) m/z 522, 524 and 526 (P+ for the 79Br, 79Br; 79Br, 81Br; 81Br, 81Br combinations, respectively, at an intensity ratio of 1:2:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639881
Source datasetuspto-grants-1997_06
ORD IDord-9034fde3a9164a89af163dfcf8e9706e
Source noteuspto-grants-1997_06