HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 18327665, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | HCID 53978782 | HCID 53978782 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18327665 | HCID 18327665 | 80% |
Reaction Steps
This compound was prepared from 4-benzyloxy-1-(3-thiocarbamoyl-benzyl)-1H-indole-2-carboxylic acid 4-(dimethylamino)-benzylamide (342 mg, 0.62 mmol), acetone (15 ml), methyl iodide (0.98 ml, 15 mmol), acetic acid (0.4 m, 0.7 mmol), ammonium acetate (809 mg, 10 mmol), and methanol (7 ml) as described in example 1/5 but the solvent for the methylation was pure acetone. The crude material was purified by flash chromatography on RP18 material with ethanol/water/acetic acid 1:1:0.1 to give 374 mg of the desired compound (80 %). M.p. 158° C. (dec.). MS: 546.2 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06337344B1 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-a0d34b4b13d64901816486ab78eb7e84 |
| Source note | uspto-grants-2002_01 |