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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304255Generated: October 25, 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/2304255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-LeucineHCID 6106—
Reactant4-Methoxy-2,3,6-trimethylbenzenesulfonyl chlorideHCID 562787—
Reactant1,1-Dimethylethyl 1-[(1-amino-6-isoquinolinyl)methyl]-2-oxo-2-(1-piperidinyl)ethyl-carbamateHCID 22665607—
ReactantN-[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—
Reactant(2S)-2-[[(4-methoxy-2,3,6-trimethylphenyl)sulfonyl]amino]-4-methylpentanoic acidHCID 57069956—
Product(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—

Reaction Steps

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, 2×d, J=7 Hz), 0.61 and 0.79 (3H, 2×d, J=7 Hz), 0.97-1.65 (9H, m), 2.13 (3H, s), 2.54 and 2.56 (3H, 2×s), 2.61 and 2.62 (3H, 2×s), 2.76-3.68 (7H, m), 3.78 and 3.84 (3H, 2×s), 4.98-5.02 and 5.18-5.22 (1H, 2×m), 6.71 (1H, s), 7.16-7.19(1H, m), 7.53-7.78 (4H, m), 8.29-8.34 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432955B1
Source datasetuspto-grants-2002_08
ORD IDord-463b2eb9afc24ee0b839626957d3e06f
Source noteuspto-grants-2002_08