HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methyl-7-nitro-1,2,3,4-tetrahydroisoquinoline hydrochloride → 1-Methyl-1,2,3,4-tetrahydroisoquinolin-7-amine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methyl-7-nitro-1,2,3,4-tetrahydroisoquinoline hydrochloride | HCID 21584310 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Methyl-1,2,3,4-tetrahydroisoquinolin-7-amine hydrochloride | HCID 21584360 | — |
Reaction Steps
A suspension of 1-methyl-7-nitro-1,2,3,4-tetrahydroisoquinoline hydrochloride (2.0 g, 8.75 mmol) in ethanol (100 ml) and a catalytic quantity of 10% Pd--C was hydrogenated until no more hydrogen was taken up. The catalyst was filtered off, the solvent was concentrated to a small volume, ether was added and the precipitated solid was collected and dried: 1.39 g (78%), MS (M+H)+ 163.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05929085 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-c2806cef2eac406a82b95c2bfaa2546c |
| Source note | uspto-grants-1999_07 |