HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 3-ethynyl-6-nitro-1-benzothiophene-2-carboxylate → Ethyl 6-amino-3-ethyl-1-benzothiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 3-ethynyl-6-nitro-1-benzothiophene-2-carboxylate | HCID 86648747 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 6-amino-3-ethyl-1-benzothiophene-2-carboxylate | HCID 67549339 | — |
Reaction Steps
Ethyl 3-ethynyl-6-nitro-1-benzothiophene-2-carboxylate obtained in Example (183d) was dissolved in methanol (16 mL) and THF (24 ml). A 10% palladium-carbon catalyst (120 mg) was added, and the mixture was stirred in a hydrogen atmosphere throughout the day. The reaction solution was filtered through celite and then concentrated under reduced pressure to obtain the title compound. The resulting compound was used for the next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08536197B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-8eb7df7d144a40ed91219e20f400af02 |
| Source note | uspto-grants-2013_09 |