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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056489Generated: November 1, 2026

Sec-Butylamine → HCID 43082197, compound

https://huagongshe.com/reaction/1056489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSec-ButylamineHCID 24874—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Fluoro-5-chlorosulfonylbenzoic acidHCID 608984—
SolventDichloromethaneHCID 6344—
ProductHCID 43082197HCID 4308219796%

Reaction Steps

5-Chlorosulfonyl-2-fluoro-benzoic acid (A, 0.506 g, 0.0021 mol), sec-butylamine (E, 0.155 g, 0.00212 mol) and DIEA (1.1 mL, 0.00636 mol) in CH2Cl2 were stirred at room temperature overnight. The solvent was evaporated and the crude product was purified by silica gel chromatography (MeOH containing 10% AcOH)/CH2Cl2) to give 5-sec-Butylsulfamoyl-2-fluoro-benzoic acid (F, 0.56 g, 96%). After drying overnight under vacuum, F (0.56 g, 0.0020 mol) in SOCl2 (5 mL) was heated at 80° C. for 3 hours, after which the SOCl2 was evaporated and the residue was dried overnight. The residue was then dissolved in tetrahydrofuran (5 mL), 3,4-difluoro-phenylamine (D, 0.26 g, 0.0020 mol) was added followed by DIEA (0.8 mL). The mixture was heated to 70° C. overnight. The solvent was evaporated, followed by ethyl acetate extraction. After purification by silica gel chromatography (ethyl acetate/hexane), 0.45 g (57%) of 5-sec-butylsulfamoyl-N-(3,4-difluoro-phenyl)-2-fluoro-benzamide (DVR-23) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399619B2
Source datasetuspto-grants-2016_07
ORD IDord-172d97d9d96340c091a8601967fccc3d
Source noteuspto-grants-2016_07