HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655663Generated: October 30, 2026
Hydrochloric Acid → HCID 16044905, compound
https://huagongshe.com/reaction/655663
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 16044904 | HCID 16044904 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 16044905 | HCID 16044905 | 71.2% |
Reaction Steps
6N-hydrochloric acid (3 ml) was added to a methanol solution (10 ml) of {4-[3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propoxy]-3-methoxy-5-methylphenyl}-carbamic acid tert-butyl ester (2.18 g, 4.3 mmol) and the mixture was stirred at room temperature overnight. After stirred at 60° C. for 15 minutes, the mixture was cooled to room temperature and a 6N aqueous sodium hydroxide solution was added thereto to neutralize it. Dichloromethane was added to the reaction mixture, and the substance extracted with dichloromethane was dried over magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:2→ethyl acetate). The purified product was concentrated to dryness under reduced pressure to obtain 4-[3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propoxy]-3-methoxy-5-methylaniline (1.26 g) as light yellow solid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08071600B2 |
|---|
| Source dataset | uspto-grants-2011_12 |
|---|
| ORD ID | ord-5950cd323e5747be959ad4741f2f655b |
|---|
| Source note | uspto-grants-2011_12 |
|---|