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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103125Generated: October 31, 2026

Piperidine → HCID 22475117, compound

https://huagongshe.com/reaction/2103125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantHCID 69059954HCID 69059954—
SolventDimethylformamideHCID 6228—
ProductHCID 22475117HCID 2247511761%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of 6-methyl-2,2-diphenyl-1,3-benzodioxole-5-carboxylic acid lithium salt (101.5 mg, 0.3 mmol) in N,N-dimethylformamide (3 mL) was added N,N,N′,N′-tetramethyl-O-(1H-benzotriazol-1-yl)-uronium-hexafluorophosphate (114 mg, 0.3 mmol, 1.0 eq.). The reaction mixture was stirred 1 h at 20° C. Piperidine (26 mg, 0.3 mmol, 1.0 eq.) was added and the reaction mixture was stirred 20 h at 20° C. The reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with water, brine and then dried over sodium sulfate, filtered and evaporated. Purification by flash chromatography afforded the title compound (73 mg, 61%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576088B2
Source datasetuspto-grants-2009_08
ORD IDord-648c34780f9244ae9d95eea19e9edc6b
Source noteuspto-grants-2009_08