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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006419Generated: October 31, 2026

Ammonium formate → HCID 10270565, compound

https://huagongshe.com/reaction/1006419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantHCID 10207065HCID 10207065—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 10270565HCID 10270565—

Reaction Steps

A mixture of 250 mg(0.54 mmole) 4-(4-benzyl-piperazin-1-yl)-1-(4-methoxybenzenesulfonyl)-1H-indole, 500 mg (8 mmole) ammonium formate and 50 mg 10% Pd-C in 20 mL ethanol was heated under reflux for 2 hours. The mixture was filtered through Whatman GF/B and the filtrate was concentrated under reduced pressure. The residue was partitioned between 10 mL 10% sodium carbonate and 25 mL ethyl acetate. The organic phase was washed with 5 ml water, 5 mL saturated sodium chloride, dried (magnesium sulfate) and concentrated under reduced pressure. The 1-(4-Methoxy-benzenesulfonyl)-4-piperazin-1-yl-1H-indole (3) was isolated as the hydrochloride salt from methanol-ethyl acetate-ether, 128 mg, m.p. 209-210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06790848B2
Source datasetuspto-grants-2004_09
ORD IDord-d191001cfea74385adf83030e9ff7162
Source noteuspto-grants-2004_09