HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86758490, compound → HCID 18434266, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86758490 | HCID 86758490 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18434266 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06441177B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-3b2da40094c44783887f3dc4b1c4c1dd |
| Source note | uspto-grants-2002_08 |