HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984451Generated: November 1, 2026
Methanesulfonyl chloride → HCID 57717560, compound
https://huagongshe.com/reaction/1984451
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 57717558 | HCID 57717558 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57717560 | HCID 57717560 | 59.4% |
Reaction Steps
Using the method of Example 66, methanesulfonyl chloride (399 mg, 3.48 mmol) was reacted with 1-(2-amino-2-methylpropyl)-2-(2-methoxyethyl)-2H-pyrazolo[3,4-c]quinolin-4-amine (1.09 g, 3.48 mmol, prepared as described in Example 590). The crude product was purified by IFC (40M cartridge eluting with a gradient of 15 to 35% CMA in chloroform) to provide a white foam. The foam was refluxed with 35% ethyl acetate in hexanes (50 mL), ethyl acetate was added until a free flowing white solid appeared, and then the mixture was cooled on ice. The solid was isolated by filtration and dried to provide 809 mg of N-{2-[4-amino-2-(methoxyethyl)-2H-pyrazolo[3,4-c]quinolin-1-yl]-1,1-dimethylethyl}methanesulfonamide as a white solid, mp 211-213° C. MS (ESI) m/z 392 (M+H)+; Anal. Calcd for C18H25N5O3S: C, 55.22; H, 6.44; N, 17.89. Found: C, 55.05; H, 6.38; N, 17.98.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07544697B2 |
|---|
| Source dataset | uspto-grants-2009_06 |
|---|
| ORD ID | ord-ed4eed1a4c434584b7ac408c74a024d4 |
|---|
| Source note | uspto-grants-2009_06 |
|---|