HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 131723093, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | HCID 54048509 | HCID 54048509 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 131723093 | HCID 131723093 | 28% |
Reaction Steps
This compound was prepared from (R)-5-benzyloxy-1-(3-thiocarbamoyl-benzyl)-1H-indole-2-carboxylic acid (1-phenyl-ethyl)-amide, methyl iodide, and ammonium acetate as described in example 1/5, but for the methylation acetone was used as solvent and in the last step methanol and acetone were used as solvents. The crude material was purified by flash chromatography on silica gel with dichloromethane/methanol/acetic acid 9:0.25:0.5 to give the desired product in 28% yield. M.p. 72° C. (dec.). MS: 503.3 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06337344B1 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-ad5dc445e30e4f298bde2d20de77e20f |
| Source note | uspto-grants-2002_01 |