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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893854Generated: November 4, 2026

Dimethylamine → (2R)-2-{(4-Chlorobenzenesulfonyl)-[4-(2-dimethylamino-acetylamino)-benzyl]-amino}-4-methyl-pentanoic acid amide

https://huagongshe.com/reaction/1893854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant(2R)-2-[[4-(2-Bromo-acetylamino)-benzyl]-(4-chlorobenzenesulfonyl)-amino]-4-methyl-pentanoic acid amideHCID 10218145—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product(2R)-2-{(4-Chlorobenzenesulfonyl)-[4-(2-dimethylamino-acetylamino)-benzyl]-amino}-4-methyl-pentanoic acid amideHCID 1021772063%

Reaction Steps

To a solution of (2R)-2-[[4-(2-bromo-acetylamino)-benzyl]-(4-chlorobenzenesulfonyl)-amino]-4-methyl-pentanoic acid amide (41 mg, 0.77 mmol) in CH2Cl2 (2 mL) was added excess 2.0 M dimethylamine in THF. The reaction mixture was stirred overnight. The solvent was removed in vacuo. Purification by flash chromatography (SiO2, 10% MeOH/CH2Cl2) afforded the title compound (24 mg) in 63% yield. MS (ESI), (M+H)+495.14, 1H NMR (CDCl3, 400 MHz) δ 8.85 (s, 1H), 8.02 (d, 2H, J=8.0), 7.75 (d, 2H, J=8.0), 7.38 (d, 2H, J=8.0), 7.29 (d, 2H, J=8.0), 6.23 (br s, 1H), 5.39 (br s, 1H), 4.62 (m, 4H), 3.25 (t, 1H, J=6.0), 2.95 (s, 6H), 1.95 (m, 1H), 1.60 (m, 2H), 0.98 (d, 3H, J=7.0), 0.94 (d, 3H, J=7.0)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513253B2
Source datasetuspto-grants-2013_08
ORD IDord-2ae1007d508f451682f263afba643d58
Source noteuspto-grants-2013_08