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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859855Generated: November 1, 2026

Methylamine → HCID 178485096, compound

https://huagongshe.com/reaction/859855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantTriethylamineHCID 8471—
ReactantHCID 86600616HCID 86600616—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178485096HCID 178485096—

Reaction Steps

40% aqueous solution of methylamine (78 mg, 1.0 mmol) was gradually added to a solution of N-(6-chloro-3-pyridylmethyl)-2-chloro-2-(4-trifluoromethylphenyl hydrazono) acetic acid amide (Compound No. 5) (0.4 g, 1 mmol) and triethylamine (0.1 g, 1 mmol) in tetrahydrofuran (10 ml) and left at room temperature overnight. Further, 40% aqueous solution of methylamine (10 mg, 0.13 mmol) was added and stirred at room temperature for 1 hour, and thereafter subjected to extraction by adding ethyl acetate and water. The organic phase was washed with a saturated brine, and then dried on anhydrous sodium sulfate. The resulting residue was purified with a silica gel chromatography to obtain N-(6-chloro-3-pyridylmethyl)-2-methylamino-2-(4-trifluoromethylphenyl hydrazono) acetic acid amide (Compound No. 191) (0.13 g, 0.34 mmol, 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153815B2
Source datasetuspto-grants-2006_12
ORD IDord-c1f95c648e3d4825bd6a0166421ec734
Source noteuspto-grants-2006_12