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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360541Generated: November 1, 2026

Boron tribromide → HCID 57717553, compound

https://huagongshe.com/reaction/1360541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 57717560HCID 57717560—
SolventDichloromethaneHCID 6344—
ProductHCID 57717553HCID 5771755356.6%

Reaction Steps

Boron tribromide (1 M in dichloromethane, 2.15 mL, 2.15 mmol) was added over a period of 2 minutes to a chilled (0° C.) slurry of N-{2-[4-amino-2-(2-methoxyethyl)-2H-pyrazolo[3,4-c]quinolin-1-yl]-1,1-dimethylethyl}methanesulfonamide (337 mg, 0.861 mmol, prepared as described in Example 592) in dichloromethane (10 mL). The reaction mixture was stirred for 14 hours and then concentrated under reduced pressure. The residue was combined with 6 M hydrochloric acid and stirred for 3 hours. The reaction mixture was diluted with 2 M aqueous sodium carbonate. The resulting precipitate was isolated by filtration and rinsed with water and chloroform. The precipitate was combined with the chloroform layer and concentrated under reduced pressure. The residue was purified by IFC (silica gel eluting with a gradient of CMA in chloroform) followed by recrystallization from ethyl acetate/hexanes/acetonitrile to provide 184 mg of N-{2-[4-amino-2-(2-hydroxyethyl)-2H-pyrazolo[3,4-c]quinolin-1-yl]-1,1-dimethylethyl}methanesulfonamide as a white solid, mp 203-204° C. MS (ESI) m/z 378 (M+H)+; Anal. Calcd for C27H23N5O3S: C, 54.09; H, 6.14; N, 18.55. Found: C, 54.11; H, 5.97; N, 18.42.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879849B2
Source datasetuspto-grants-2011_02
ORD IDord-c7ce020acc2c4d72b1e5dc6bb0d2a935
Source noteuspto-grants-2011_02