HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505529Generated: October 31, 2026
HCID 44479178, compound → HCID 86702968, compound
https://huagongshe.com/reaction/1505529
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 44479178 | HCID 44479178 | — |
| Reactant | HCID 86702965 | HCID 86702965 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86702968 | HCID 86702968 | 82% |
Reaction Steps
The N-(3-amino-2,4-difluorophenyl)-1-methyl-1H-imidazole-4-sulfonamide (45 mg, 0.16 mmol) prepared at Step 5 and the 6-(2-fluoropyridin-3-yl)-9-(tetrahydro-2H-pyran-2-yl)-9H-purine (43 mg, 0.14 mmol) prepared at Step 7 were added and dissolved, and lithium (bistrimethylsilyl) amide (1.0M solution in THF) was applied slowly at 0° C. After stirring the reactant at room temperature for 1 hour, completing the reaction, pouring water, and extracting with ethylacetate, the organic layer was dried with sulfuric anhydride magnesium and vacuum concentrated, and then refined by means of column chromatography, so that 65 mg of the target compound, N-(2,4-difluoro-3-(3-(9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl)pyridin-2-ylamino)phenyl)-1-methyl-1H-imidazole-4-sulfonamide (percentage yield: 82%), was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09216981B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-5a76149d22874f379ef538bf3aa0d5b9 |
|---|
| Source note | uspto-grants-2015_12 |
|---|