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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958717Generated: October 31, 2026

Triethylamine → (R)-benzyl 4-(dimethylamino)-3-(6-phenoxypyridine-3-sulfonamido)butanoate

https://huagongshe.com/reaction/1958717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant6-Phenoxypyridine-3-sulphonyl chlorideHCID 2776499—
Reactant(R)-benzyl 3-amino-4-(dimethylamino)butanoateHCID 46223508—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(R)-benzyl 4-(dimethylamino)-3-(6-phenoxypyridine-3-sulfonamido)butanoateHCID 8664121637%

Reaction Steps

To a solution of (R)-benzyl 3-amino-4-(dimethylamino)butanoate (32 mg, 0.086 mmol), triethylamine (50 μL, 0.36 mmol) and DMAP (1 mg, 0.008 mmol) in anhydrous CH2Cl2 (1 mL) was added 6-phenoxypyridine-3-sulfonyl chloride is reacted with R-aminocarnitine benzyl ester (67 mg, 0.25 mmol). The solution was stirred overnight at room temperature. The solvents were removed in vacuo and the residue was purified by preparatory HPLC. The residue was dissolved into CH2Cl2 (50 mL) and washed with 0.1 N NaOH (5 mL), dried over MgSO4 and concentrated to give the title compound as a white solid (18 mg, 37%). MS ESI 470.2 [M+H]+, calcd for [C24H27N3O5S+H]+ 470.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410150B2
Source datasetuspto-grants-2013_04
ORD IDord-27259aa0d0d2491cac48a051db30f0f0
Source noteuspto-grants-2013_04