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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 636933Erstellt: 26. Oktober 2026

L-Leucine → (2S)-N-[1-[(1-amino-6-isoquinolinyl)methyl]-2-oxo-2-(1-piperidinyl)ethyl]-2-[[(4-methoxy-2,3,6-trimethylphenyl)sulfonyl]amino]-4-methylpentanamide hydrochloride

https://huagongshe.com/reaction/636933

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktL-LeucineHCID 6106—
Edukt4-Methoxy-2,3,6-trimethylbenzenesulfonyl chlorideHCID 562787—
Edukt1,1-Dimethylethyl 1-[(1-amino-6-isoquinolinyl)methyl]-2-oxo-2-(1-piperidinyl)ethyl-carbamateHCID 22665607—
EduktN-[1-[(1-Amino-6-isoquinolinyl)methyl]-2-oxo-2-(1-piperidinyl)ethyl]-2-[[(3,4-dihydro-2,2,5,7,8-pentamethyl-2H-1-benzopyran-6-yl)sulfonyl]amino]acetamide hydrochlorideHCID 22665631—
Edukt(2S)-2-[[(4-methoxy-2,3,6-trimethylphenyl)sulfonyl]amino]-4-methylpentanoic acidHCID 57069956—
Produkt(2S)-N-[1-[(1-amino-6-isoquinolinyl)methyl]-2-oxo-2-(1-piperidinyl)ethyl]-2-[[(4-methoxy-2,3,6-trimethylphenyl)sulfonyl]amino]-4-methylpentanamide hydrochlorideHCID 86588688—

Reaktionsschritte

The procedure described for 5c was used. Deprotection of 75 mg of 5a and coupling with 72 mg of (2S)-2-[[(4-methoxy-2,3,6-trimethylphenyl)sulfonyl]amino]-4-methylpentanoic acid (prepared from L-leucine and 4-methoxy-2,3,6-trimethylphenylsulfonylchloride using the procedure described for 5b) yielded after purification the title compound (65 mg) as a mixture of diastereomers (1:1). 1H-NMR 400 MHz (CD3OD) δ: 0.50 and 0.68 (3H, 2x d, J=7 Hz), 0.61 and 0.79 (3H, 2x d, J=7 Hz), 0.97-1.65 (9H, m), 2.13 (3H, s), 2.54 and 2.56 (3H, 2x s), 2.61 and 2.62 (3H, 2x s), 2.76-3.68 (7H, m), 3.78 and 3.84 (3H, 2x s), 4.98-5.02 and 5.18-5.22 (1H, 2x m), 6.71 (1H, s), 7.16-7.19 (1H, m), 7.53-7.78 (4H, in), 8.29-8.34 (1H, m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06194409B1
Quelldatensatzuspto-grants-2001_02
ORD IDord-a49d65451dcd480789a86fc147049497
Quellennotizuspto-grants-2001_02