HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 20284821, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-(2,3,4,9-Tetrahydrothiopyrano[2,3-b]indol-4-yl)methanamine | HCID 3056088 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium cyanoborohydride | HCID 5003444 | — |
| Product | HCID 20284821 | HCID 20284821 | 99.1% |
Reaction Steps
To a solution of 4-aminomethyl-2,3,4,9-tetrahydrothiopyrano[2,3-b]indole (150 mg) in methanol (5 ml) are added a solution of benzaldehyde (76 mg) in methanol (1.5 ml) and sodium cyanoborohydride (132 mg). The mixture is adjusted to pH 7 with a solution of hydrochloride in methanol, stirred at room temperature for 1 hour and evaporated to remove the solvent. The residue is dissolved in ether, washed with a 10% aqueous solution of sodium hydroxide and a saline solution, dried and evaporated to give the title compound (210 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04256640 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-84dee13c01884284825e175ee3d51cf3 |
| Source note | uspto-grants-1981_03 |