HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 68673728, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Benzyl-4-piperidylamine | HCID 415852 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2,3-Dihydro[1,4]dioxino[2,3-c]pyridine-7-carbaldehyde | HCID 21873668 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium hydroxide methanol | HCID 23721981 | — |
| Product | HCID 68673728 | HCID 68673728 | — |
Reaction Steps
A solution of 3.0 g of 2,3-dihydro-(1,4)dioxino(2,3-c)pyridin-7-carbaldehyde and 3.4 g of 4-amino-1-benzylpiperidine in 30 mL of methanol was stirred for 50 minutes at room temperature, and a solution of 0.34 g of sodium borohydride in 30 mL of 0.01 mol/L sodium hydroxide/methanol was added dropwise thereto under ice cooling. The mixture was further stirred for 2 hours under ice cooling, 6 mL of concentrated hydrochloric acid was added dropwise thereto at 10° C. or lower and stirred for 1 hour 30 minutes. The solid product was obtained by filtration to give 6.8 g of 1-benzyl-N-(2,3-dihydro-(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)piperidin-4-amine trihydrochloride as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354426B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-0d14b781491a4978a5ab15c0bf2dad4d |
| Source note | uspto-grants-2013_01 |