HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole-3-Acetic Acid → (3aRS,4RS,5RS,7aSR)-4-(2-methoxyphenyl)-2-(3-indolylacetyl)-5-methyl-4-perhydroisoindolol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole-3-Acetic Acid | HCID 802 | — |
| Reactant | 4-(2-Methoxyphenyl)-5-methyl-4-perhydroisoindolol | HCID 67714350 | — |
| Product | (3aRS,4RS,5RS,7aSR)-4-(2-methoxyphenyl)-2-(3-indolylacetyl)-5-methyl-4-perhydroisoindolol | HCID 67714321 | 39.5% |
Reaction Steps
By working according to the experimental procedure of Example 16, from 1.21 g of 3-indoleacetic acid and 1.39 g of (3aRS,4RS,5RS,7aSR)-4-(2 -methoxyphenyl)-5-methyl-4-perhydroisoindolol, and after purification on a column of silica gel (particle size 0.04-0.06 mm, diameter 2.8 cm, height 25 cm), eluting under a pressure of 0.5 bar of nitrogen with a mixture of cyclohexane and ethyl acetate (40/60 by volume), 0.88 g of (3aRS,4RS,5RS,7aSR)-4-(2-methoxyphenyl)-2-(3-indolylacetyl)-5-methyl-4-perhydroisoindolol is obtained in the form of a white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05624950 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-ddebf3c3d5504bc09ec4e9bae809e946 |
| Source note | uspto-grants-1997_04 |