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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306489Generated: October 31, 2026

HCID 86758490, compound → HCID 18434266, compound

https://huagongshe.com/reaction/2306489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86758490HCID 86758490—
SolventDichloromethaneHCID 6344—
ProductHCID 18434266HCID 18434266—

Reaction Steps

The fumarate obtained is taken up in methylene chloride/saturated sodium bicarbonate solution and the organic phase is dried and concentrated. 3.09 g of the thus-obtained [4-[6-(allyl-methyl-amino)-hexyloxy]-2-methoxy-phenyl]-(4-bromo-phenyl)-methanone are boiled in 13 ml of acetic acid/7.7 ml of 62% HBr solution at 90° C. for 2 hrs. The reaction mixture is concentrated and the residue is converted into the free base with methylene chloride/saturated sodium bicarbonate solution. The residue is treated with 0.74 g of fumaric acid and processed using ethanol/ether. There are obtained 2.05 g of [4-[6-(allyl-methyl-amino)-hexyloxy]-2-hydroxy-phenyl]-(4-bromo-phenyl)-methanone fumarate, MS: m/e 446 (M+H+, 1Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441177B1
Source datasetuspto-grants-2002_08
ORD IDord-3b2da40094c44783887f3dc4b1c4c1dd
Source noteuspto-grants-2002_08