HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426075Generated: October 27, 2026
Potassium Carbonate → 4-(2,5-Difluoro-phenylamino)-6-[4-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-piperidin-1-yl]-pyrimidine-5-carbonitrile
https://huagongshe.com/reaction/1426075
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,5-Difluoroaniline | HCID 67775 | — |
| Reactant | 4,6-Dichloropyrimidine-5-carbonitrile | HCID 599371 | — |
| Reactant | 4-(3-(Propan-2-yl)-1,2,4-oxadiazol-5-yl)piperidine | HCID 24208845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(2,5-Difluoro-phenylamino)-6-[4-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-piperidin-1-yl]-pyrimidine-5-carbonitrile | HCID 58216415 | — |
Reaction Steps
To a solution of 4,6-Dichloro-pyrimidine-5-carbonitrile (254 mg, 1.47 mmol) and 2,5-difluoroaniline (190 mg, 1.47 mmol) in DMF (3 mL) at 0° C. was added K2CO3 (203 mg, 1.47 mmol) The completion of the reaction was monitored by TLC (EtOAc:Hex=1:1, Rf=0.90). After the reaction was complete, 4-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-piperidine (340 mg, 1.47 mmol) and K2CO3 (406 mg, 2.94 mmol) were added at 0° C. The reaction was warmed to rt and stirred for 30 min. The reaction was heated to 40° C. and maintained for 1 h. The reaction was cooled to rt, poured in to H2O (50 mL) and extracted with EtOAc (50 mL, two times). The EtOAc was dried over MgSO2 and concentrated under vacuum. The crude product was purified over SiO2 (EtOAc:Hex=1:1, Rf=0.44) to afford the desired Compound B131 (465 mg; 71.1%). 1H-NMR (DMSO-d6): 9.32 (1H, s), 8.19 (1H, s), 7.40-7.08 (3H, m), 4.54 (2H, m), 3.48-3.32 (4H, m), 3.07-3.01 (2H, m), 2.18-2.14 (2H, b), 1.96-1.86 (2H, m), 1.27 (6H, d) ppm. LCMS: 426.43.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933083B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-f6e45539f951422580dcd89bc009d832 |
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| Source note | uspto-grants-2015_01 |
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