HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 10367633, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(3-amino-5-tert-butyl-2-methoxy-phenyl)-methanesulfonamide | HCID 10214710 | — |
| Reactant | 1-Methyl-7-nitroindole-2-carboxylic acid | HCID 57722444 | — |
| Product | HCID 10367633 | HCID 10367633 | 87% |
Reaction Steps
A suspension of 1-methyl-7-nitroindole-2-carboxylic acid (220 mg, 1 mmol) in 5 mL of SO2Cl was heated at reflux for 3 h to give a yellow solution. The excess SO2Cl was removed by distillation and the resulting yellow solid was dissolved in 5 mL of dry THF. Et3N (0.21 mL, 1.5 mmol) and N-(3-amino-5-tert-butyl-2-methoxy-phenyl)-methanesulfonamide (327 mg, 1.2 mmol) were added successively and the mixture was stirred 12 h. The reaction mixture was extracted with EtOAc to give 410 mg (87%) of 1-methyl-7-nitroindole-2-carboxylic acid (5-tert-butyl-3-methanesulfonylamino-2-methoxy-phenyl)-amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07550461B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-5cc62054f5ab461a901888daa79f32c1 |
| Source note | uspto-grants-2009_06 |