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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908685Generated: October 27, 2026

Dimethylformamide → HCID 131731063, compound

https://huagongshe.com/reaction/1908685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCesium carbonateHCID 10796—
ReactantN,N-dimethylhydroxylamine hydrochlorideHCID 27969—
ReactantHCID 71487163HCID 71487163—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 131731063HCID 131731063—

Reaction Steps

(1S,2S)-2-Phenyl-cyclopropanecarboxylic acid [(S)-1-(6-chloro-pyridin-3-yl)-ethyl]-amide (Compound 18) (2.00 g, 6.65 mmol) was dissolved in DMF (40 ml). N,N-dimethylhydroxylaminehydrochloride (5.00 g, 51.2 mmol) and dicesium carbonate (25 g, 76.7 mmol) were added and the mixture was heated at 95 C 3 days. The mixture was poured out into brine and extracted with EtOAc. The organic layer was washed with brine, dried (MgSO4) and was filtered and then evaporated to dryness. The residue was transferred to a silica gel column and eluded with EtOAc to give Compound 50 as a solid. This solid was dissolved in a mixture of THF (10 ml), EtOAc (10 ml) and heptanes (10 ml). The mixture was concentrated to approx. 10 ml volume and this solution was cooled in an ice/water bath. A white precipitate formed. The solids was collected by filtration and dried in vacuo to give the title compound as a white solid (0.044 g, 2%). 1H-NMR (500 MHz, DMSO) δ 8.43 (d, 1H), 8.02 (s, 1H), 7.45 (d, 1H), 7.25 (m, 2H), 7.17 (m, 1H), 7.10 (d, 2H), 6.61 (d, 1H), 4.83 (m, 1H), 3.98 (m, 6H), 2.19 (m, 1H), 1.90 (m, 1H), 1.35 (m, 4H), 1.21 (m, 1H). LC-MS (m/z) 310.2 (MH+), tR=0.46 min (method B). Mp=171-181 C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598213B2
Source datasetuspto-grants-2013_12
ORD IDord-68d70c629bed4913b64f2ff45e299b6c
Source noteuspto-grants-2013_12