HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233981Generated: October 31, 2026
Methanesulfonyl chloride → HCID 86608328, compound
https://huagongshe.com/reaction/2233981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 86608329 | HCID 86608329 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86608328 | HCID 86608328 | 30.1% |
Reaction Steps
Methane sulfonyl chloride (0.032 ml, 0.412 mmol) was added dropwise to a solution of 2-(2-aminoethoxy)-6-(4-{[(3,4-dichloro-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)-N-methoxypyrimidine-4-carboxamide (Example 319, 0.20 g, 0.412 mmol), TEA (0.11 ml, 0.824 mmol) and DMF (3 ml) at 0° C. The reaction was stirred for 15 minutes at 0° C. then quenched with water. The aqueous phase was extracted with EtOAc, washed with saturated sodium bicarbonate solution, water and brine. It was dried over magnesium sulfate and concentrated to give brown solid, which was purified by reverse phase HPLC (30% to 35% acetonitrile in water, 0.1% TFA) affording the title compound (70 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07709503B2 |
|---|
| Source dataset | uspto-grants-2010_05 |
|---|
| ORD ID | ord-54dc5dacab23492487734cd377416ef9 |
|---|
| Source note | uspto-grants-2010_05 |
|---|