HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 13561992, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 11085189 | HCID 11085189 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13561992 | HCID 13561992 | — |
Reaction Steps
In the same manner as described in Example 53, (3RS)-1,2,3,4-tetrahydro-β-carboline-3-carboxamide (0.71 g), triethylamine (0.46 ml), carbon disulfide (0.22 ml), 70% ethanol (20 ml) and methyl iodide (0.22 ml) are reacted and treated. The product is crystallized from ethyl acetate to give the title compound (0.414 g), m.p. 224°-225° C. (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04628057 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-3655041b0fee4fbfb804794b9e3c85f5 |
| Source note | uspto-grants-1986_12 |