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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584893Generated: November 1, 2026

Dichloromethane → HCID 57085494, compound

https://huagongshe.com/reaction/1584893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 21221013HCID 21221013—
ProductHCID 57085494HCID 57085494—

Reaction Steps

Trifluoroacetic acid (10 ml) was added to a solution of N-[(1-tert-butoxycarbonyl-4-piperidyl)methyl]pyridine-3-carboxamide (1.56 g) in dichloromethane (25 ml) and the mixture stirred for 2 hours then the solvent was removed in vacuo. The residue was dissolved in dry acetonitrile (10 ml) and potassium carbonate (5.0 g) was added, followed by a solution of (R)-7-chloro-1,4-benzodioxan-2-ylmethyl 4-toluenesulphonate (1.7 g) in dry acetonitrile (15 ml), and the mixture was stirred and heated under reflux for 6 hours. The cooled mixture was poured into water then extracted with dichloromethane (2×100 ml). The combined extracts were washed with brine (100 ml), dried over magnesium sulphate, and the solvent removed in vacuo. The residue was purified by flash chromatography over silica eluting with a 20:1 mixture of dichloromethane and methanol. Appropriate fractions were combined and the solvent removed in vacuo to give (S)-N-{[1-(8-chloro-1,4-benzodioxan-2-ylmethyl)-4-piperidyl]methyl}pyridine-3-carboxamide (1.04 g) as a colourless solid m.p. 52-54° C. [α]D -35.3° (c=1.024, methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935973
Source datasetuspto-grants-1999_08
ORD IDord-c13717a3418a4a2995b000475a84f712
Source noteuspto-grants-1999_08