HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Propenoyl chloride, 3-(3,4,5-trimethoxyphenyl)-, (2E)- → 5,6,13,13a-tetrahydro-2,3,11-trimethoxy-10-(3', 4', 5'-trimethoxycinnamoyloxy)-8H-dibenzo[a, g]quinolizine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Propenoyl chloride, 3-(3,4,5-trimethoxyphenyl)-, (2E)- | HCID 112094 | — |
| Reactant | 10-hydroxy-2,3,11-trimethoxy-5,6,13,13a-tetrahydro-8H-dibenzo[a, g]quinolizine hydrochloride | HCID 86732983 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5,6,13,13a-tetrahydro-2,3,11-trimethoxy-10-(3', 4', 5'-trimethoxycinnamoyloxy)-8H-dibenzo[a, g]quinolizine | HCID 86732985 | 46.4% |
Reaction Steps
1.9 g of 10-hydroxy-2,3,11-trimethoxy-5,6,13,13a-tetrahydro-8H-dibenzo[a, g]quinolizine hydrochloride was treated in the same manner as described in Example 6, using 2.0 g of 3,4,5-trimethoxycinnamoyl chloride and 20 ml of anhydrous pyridine and there was obtained 1.3 g (46.4% yield) of 5,6,13,13a-tetrahydro-2,3,11-trimethoxy-10-(3', 4', 5'-trimethoxycinnamoyloxy)-8H-dibenzo[a, g]quinolizine as a pale yellow powder. The methiodide derived from this compound was found to be in agreement with the methiodide of the compound obtained in Example 5 as determined from the melting point and IR spectrum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03933826 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-47292063710140caa1214a1d5fff1ce6 |
| Source note | uspto-grants-1976_01 |