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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005662Generated: November 1, 2026

Formaldehyde → Ro4368554

https://huagongshe.com/reaction/1005662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantHCID 69351600HCID 69351600—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductRo4368554HCID 6918682—

Reaction Steps

A solution of 3-benzenesulfonyl-7-piperazin-1-yl-1H-indole (101) (500 mg, 1.46 mmol) and 1 mL of 37% aqueous formaldehyde in 25 mL of ethanol was hydrogenated at atmospheric pressure in the presence of 250 mg of 10% Pd-C for 30 min. The mixture was filtered, diluted with water and extracted with ethyl acetate. The ethyl acetate was washed with water and brine, dried, and evaporated to yield the crude free base of 3-benzenesulfonyl-7-(4-methyl-piperazin-1-yl)-1H-indole. The hydrochloride salt was crystallized from ethanol-ether to afford 290 mg of (501), m.p. 160-162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787535B2
Source datasetuspto-grants-2004_09
ORD IDord-3a751f096c5a485a935238028a02882b
Source noteuspto-grants-2004_09