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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984451Generated: November 1, 2026

Methanesulfonyl chloride → HCID 57717560, compound

https://huagongshe.com/reaction/1984451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 57717558HCID 57717558—
SolventEthyl AcetateHCID 8857—
ProductHCID 57717560HCID 5771756059.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544697B2
Source datasetuspto-grants-2009_06
ORD IDord-ed4eed1a4c434584b7ac408c74a024d4
Source noteuspto-grants-2009_06