HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522907Generated: October 30, 2026
Cesium carbonate → 4-(4-(3-(2,4-dichlorophenoxy)azetidin-1-yl)pyrimidin-2-ylamino)-N-methylbenzamide
https://huagongshe.com/reaction/522907
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Amino-N-methylbenzamide | HCID 235516 | — |
| Reactant | 2-Chloro-4-(3-(2,4-dichlorophenoxy)azetidin-1-yl)pyrimidine | HCID 86685255 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 4-(4-(3-(2,4-dichlorophenoxy)azetidin-1-yl)pyrimidin-2-ylamino)-N-methylbenzamide | HCID 67355164 | 29% |
Reaction Steps
To a solution of 2-chloro-4-(3-(2,4-dichlorophenoxy)azetidin-1-yl)pyrimidine (0.200 g, 609 mmoL) and 4-amino-N-methylbenzamide (0.109 g, 0.731 mmoL) in dimethyl acetamide (5 mL) was added cesium carbonate (300 mg, 9.14 mmol) and the reaction mixture was degassed for 15 min. Tris(dibenzylideneacetone)dipalladium (0) [Pd2(dba)3](0.030 g, 0.03 mmoL) and 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl [BINAP] (0.020 g, 0.03 mmoL) were added and the mixture was irradiated in the microwave at 120° C. for 1 h. Then the reaction was quenched with water and extracted with EtOAc (2×25 mL). The organic extracts were washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. Purification by silica gel column chromatography provided 4-(4-(3-(2,4-dichlorophenoxy)azetidin-1-yl)pyrimidin-2-ylamino)-N-methylbenzamide (0.077 g, 29%) as solid. Observed mass (M+1): 443.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09334269B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-eede4a1393374044915130319e99f6f7 |
|---|
| Source note | uspto-grants-2016_05 |
|---|