HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl trans 5-chloro-2-(phenylsulfonylamino)cinnamate → Methyl[5-chloro-2-(4-methoxypyridine-2-carbonyl)-1h-indol-3-yl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl trans 5-chloro-2-(phenylsulfonylamino)cinnamate | HCID 11187263 | — |
| Reactant | 2-Bromoacetyl-4-methoxypyridine hydrobromide | HCID 23003305 | — |
| Product | Methyl[5-chloro-2-(4-methoxypyridine-2-carbonyl)-1h-indol-3-yl]acetate | HCID 23003520 | — |
Reaction Steps
The title compound was prepared according to the procedure described in Example 57 from methyl trans-5-chloro-2-(penylsulfonylamino)cinnamate (Example 36, step 3) and 2-bromoacetyl-4-methoxypyridine hydrobromide (Preparation is described in Example 105).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06608070B1 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-0a5f053ae4994e918dfee3f1c569d1a4 |
| Source note | uspto-grants-2003_08 |