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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252172Generated: October 30, 2026

Methylamine → (2S)-[4-(4-Aminobutyl)benzenesulfonylamino]-3-methylbutyramide

https://huagongshe.com/reaction/252172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant(2S)-{4-[4-(1,3-Dioxo-1,3-dihydroisoindol-2-yl)butyl]benzenesulfonylamino}-3-methylbutyramideHCID 58912945—
Product(2S)-[4-(4-Aminobutyl)benzenesulfonylamino]-3-methylbutyramideHCID 5864957954.8%

Reaction Steps

A mixture of (2S)-{4-[4-(1,3-dioxo-1,3-dihydroisoindol-2-yl)butyl]-benzenesulfonylamino}-3-methylbutyramide 14 (0.40 g, 0.87 mmol) and methylamine (2 M in methanol, 20 mL, 40 mmol) was stirred at room temperature overnight. Solvent was removed by rotary evaporation and the residue was purified by flash silica gel column chromatography eluting with chloroform/methanol/concentrated ammonium hydroxide (3:1:0.1, v/v) to give (2S)-[4-(4-aminobutyl)benzenesulfonylamino]-3-methyl-butyramide (15) as a white powder (156 mg, 54% yield). 1H NMR (300 MHz, CD3OD) δ 0.85 (d, 3H), 0.87 (d, 3H), 1.66 (m, 4H), 1.90 (m, 1H), 2.69 (m, 4H), 3.51 (d, 1H), 7.35 (d, 2H) 7.75 (d, 2H). m/z (ESI): 328 [C15H25N3O3S+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868010B2
Source datasetuspto-grants-2011_01
ORD IDord-bf26d507cf9d4ce7a8331b5ac26bf53a
Source noteuspto-grants-2011_01