HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 131712929, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | N-Butyl-1H-indole-3-ethanamine | HCID 45582 | — |
| Reactant | HCID 20513196 | HCID 20513196 | — |
| Product | HCID 131712929 | HCID 131712929 | — |
| Product | HCID 131712930 | HCID 131712930 | — |
Reaction Steps
To a solution of 3.4 g of N-n-butyl-tryptamine in 50 ml of toluene are added 4.6 g of N-methyl-N-benzyloxycarbonyl-2-aminopropionaldehyde, and the mixture is refluxed for 15 hours. After the reaction, the mixture is condensed under reduced pressure. Then, the residue obtained is purified by silica gel chromatography. 3.9 g of 1,2,3,4-tetrahydro-1-(2-N-methyl-N-benzyloxycarbonylamino)ethyl)-2-n-butyl-β-carboline (cis isomer) and 1.32 g of 1,2,3,4-tetrahydro-1-(2-(N-methyl-N-benzyloxycarbonylamino)ethyl-2-n-butyl-β-carboline (trans isomer) are obtained, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04367230 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-b3e85bcbf88e47baa43e6bc954019c97 |
| Source note | uspto-grants-1983_01 |