HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201098Generated: October 29, 2026
Cesium carbonate → tert-butyl 2-(1H-pyrazol-1-yl)pyridin-4-ylcarbamate
https://huagongshe.com/reaction/2201098
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | tert-Butyl carbamate | HCID 77922 | — |
| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Reactant | 4-Bromo-2-(1H-pyrazol-1-yl)pyridine | HCID 45787902 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | tert-butyl 2-(1H-pyrazol-1-yl)pyridin-4-ylcarbamate | HCID 67514899 | — |
Reaction Steps
Commercial 4-bromo-2-(1H-pyrazol-1-yl)pyridine (500 mg, 2.23 mmol) was dissolved in 30 mL dioxane. To it were added t-butyl carbamate (392 g, 3.35 mmol), cesium carbonate (1.46 g, 4.46 mmol), Pd2(dba)3 (101 mg, 0.11 mmol) and XantPhos (192 mg, 0.33 mmol). The mixture was degassed with Ar stream and stirred under Ar in 85° C. bath for overnight. The mixture was concentrated, taken into 200 mL EtOAc and 100 mL water. The organic phase was separated, dried, concentrated and subjected to flash column (0-20% EtOAc in DCM) to obtain tert-butyl 2-(1H-pyrazol-1-yl)pyridin-4-ylcarbamate. This compound was treated with 2:1 DCM/TFA mixture at RT for 2 h. The mixture was pumped to dryness to afford 2-(1H-pyrazol-1-yl)pyridin-4-amine di-TFA salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09359375B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-1a07a6d6051343858889682a1b41a04f |
|---|
| Source note | uspto-grants-2016_06 |
|---|