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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398353Generated: November 3, 2026

Methylamine → 2-Acetamido-8-chloro-6-methylbenzo[c][2,7]naphthyridin-6-ium fluoride

https://huagongshe.com/reaction/1398353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantN-(4-(4-chloro-2-fluorophenyl)-5-formylpyridin-2-yl)acetamideHCID 86695932—
SolventDichloromethaneHCID 6344—
Product2-Acetamido-8-chloro-6-methylbenzo[c][2,7]naphthyridin-6-ium fluorideHCID 8671034693.1%

Reaction Steps

To a stirred solution of N-(4-(4-chloro-2-fluorophenyl)-5-formylpyridin-2-yl)acetamide (0.39 g, 1.332 mmol) and 4 Å molecular sieves (50 mg) in dichloromethane (35 mL) at 0° C. was added methyl amine (8M in EtOH, 0.041 g, 0.166 mL, 1.332 mmol) dropwise and the reaction was stirred at rt overnight (12 h). The reaction mixture was diluted with DCM (40 mL) and filtered through a bed of diatomaceous earth (Celite®). The filtrate was concentrated under reduced pressure to afford 2-acetamido-8-chloro-6-methylbenzo[c][2,7]naphthyridin-6-ium fluoride (450 mg, 1.24 mmol, 93% yield) as a yellow solid that was used in the next step without purification. LC/MS (ESI) m/e 286.1 [(M)+, calcd for C15H13ClN3O 286.1]; LC/MS retention time (Method D): tR=0.71 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901305B2
Source datasetuspto-grants-2014_12
ORD IDord-73f6d047097d4459b3816b9c2180cded
Source noteuspto-grants-2014_12