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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872660Generated: October 27, 2026

Piperidine → Farampator

https://huagongshe.com/reaction/1872660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant2,1,3-Benzoxadiazole-5-carboxylic acidHCID 2735454—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
SolventDichloromethaneHCID 6344—
ProductFarampatorHCID 4118151—

Reaction Steps

Benzofurazan-5-carboxylic acid (2.0 g, 12.2 mmol) was suspended in 10 mL dichloromethane. Carbonyl diimidazole (2.0 g, 12.3 mmol) was added, which caused dissolution with gas evolution. The resulting yellow solution was stirred for 40 minutes at room temperature, following which, piperidine (1.2 g, 14.1 mmol) was added. The solution was stirred overnight and then concentrated onto silica. Product was eluted with hexane/ethyl acetate (2:1) and purified by distillation in a kugelrohr at 155-170° C. and 0.5 mmHg. 1-(Benzofurazan-5-ylcarbonyl)piperidine, 2 (2.78 g, 99%), initially a pale yellow oil, crystallized upon cooling. M.p. 88.5-90.5° C. IR: 2938, 2857, 1630, 1519, 1439, 1266, 1223, 996, 881, 816, and 740 cm-1. 1H NMR (500 MHz): δ 7.90 (1H, d, J=9.7 Hz); 7.84 (1H, s); 7.44 (1H, dd, J=9.4 and 1.4 Hz); 3.74 (2H, br s); 3.39 (2H, br s); 1.72 (4H, br s); and 1.57 ppm (2H, br s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06110935
Source datasetuspto-grants-2000_08
ORD IDord-84b5bb45f32a458b87faf35b9b4359e8
Source noteuspto-grants-2000_08