HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474014Generated: October 30, 2026
Diisopropylamine → HCID 178428353, compound
https://huagongshe.com/reaction/474014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 4,6-Dichloro-5-fluoro-2-methanesulfonylpyrimidine | HCID 86616257 | — |
| Reactant | HCID 178418690 | HCID 178418690 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178428353 | HCID 178428353 | — |
Reaction Steps
To a solution of 4,6-dichloro-5-fluoro-2-(methylsulfonyl)pyrimidine in THF (25 ml) was added diisopropylamine (1.32 g, 10.20 mmol, 1.82 ml) and 3-methyl-1H-pyrazol-5-amine (1.04 g, 10.71 mmol) and the mixture stirred at room temperature for 30 mins. The reaction was diluted with ethyl acetate (100 ml) and water (100 ml), the organic layer was washed with brine (50 ml), dried (Na2SO4), and partially concentrated until a solid started to precipitate. The suspension was cooled in an ice bath for 1 hr and filtered to give the title compound as a pale yellow solid. A second crop was obtained by leaving the filtrate to stand overnight (total 1.55 g, 50%). 1H NMR (DMSO, 400 MHz) 2.26 (3H, s), 3.32 (3H, s), 6.48 (1H, s), 11.03 (1H, s), 12.35 (1H, s) ES+306.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08637511B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-2b4916e28677498899dba0e3f0ada9f3 |
|---|
| Source note | uspto-grants-2014_01 |
|---|