HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → tert-butyl 6-bromo-1H-pyrazolo[4,3-b]pyridine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | 6-Bromo-1H-pyrazolo[4,3-b]pyridine | HCID 40152259 | — |
| Reactant | tert-Butyl 5-bromo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate | HCID 50986454 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | tert-butyl 6-bromo-1H-pyrazolo[4,3-b]pyridine-1-carboxylate | HCID 86715472 | 93% |
Reaction Steps
Analogous to the preparation of tert-butyl 5-bromo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate, 6-bromo-1H-pyrazolo[4,3-b]pyridine (2.0 g, 10.10 mmol) was reacted with di-tert-butyl dicarbonate (2.8 g, 13.10 mmol), NEt3 (1.44 g, 2.0 mL, 14 mmol) and 4-(dimethylamino)pyridine in acetonitrile (20 mL) for 3 h. Work-up as discussed previously in the preparation of tert-butyl 5-bromo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate provided desired product of tert-butyl 6-bromo-1H-pyrazolo[4,3-b]pyridine-1-carboxylate as a brown solid (2.8 g, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09145433B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-5aab59fe29124a0b8ad8dbb22356177a |
| Source note | uspto-grants-2015_09 |