HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoacetyl-4-ethylpyridine → Methyl[2-(4-ethylpyridine-2-carbonyl)-5-trifluoromethoxy-1h-indol-3-yl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoacetyl-4-ethylpyridine | HCID 23003263 | — |
| Reactant | Methyl trans-2-p-toluenesulfonylamino-5-(trifluoromethoxy)cinnamate | HCID 23003398 | — |
| Product | Methyl[2-(4-ethylpyridine-2-carbonyl)-5-trifluoromethoxy-1h-indol-3-yl]acetate | HCID 23003375 | — |
Reaction Steps
The title compound was prepared according to the procedure described in Example 57 from methyl trans-2-p-toluenesulfonylamino-5-(trifluoromethoxy)cinnamate (step 2 of Example 145) and 2-bromoacetyl-4-ethylpyridine (Preparation is described in Example 57).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06608070B1 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-88e2dc5bfef94fd5999160405cf22f1c |
| Source note | uspto-grants-2003_08 |