Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | HCID 21506620 | HCID 21506620 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21506608 | HCID 21506608 | — |
Reaction Steps
4.48 g. of α-(3,4,5-trimethoxybenzamido)-N-[2-hydroxy-2-(3,4-dimethoxyphenyl)-ethyl]-acetamide [producible from 2-(3,4-dimethoxyphenyl)-2-hydroxyethylamine and 3,4,5-trimethoxybenzamidoacetyl chloride] is allowed to stand in 100 ml. of chloroform with 6.2 g. of phosphorus pentachloride for 3 days at 20°. The mixture is decomposed with ice water and washed several times with NaHCO3 solution. The chloroform solution is evaporated. The thus-obtained crude 1-(3,4,5-trimethoxybenzamidomethyl)-6,7-dimethoxy-isoquinoline is taken up in 50 ml. of methanol, combined with 400 mg. of PtO2, and hydrogenated at 20° and under normal pressure. The product is filtered and evaporated. Chromatography on silica gel (with chloroform/methanol 19:1) yields 1-(3,4,5-trimethoxybenzamidomethyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline; hydrochloride, m.p. 234°-236°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03985881 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-9825351244b54d71aaae1b13dc5d2394 |
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| Source note | uspto-grants-1976_10 |
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