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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743429Generated: October 27, 2026

2-(N-carbobenzyloxyaminosulfonyl)aminopentanoic acid methyl ester → 2-(Aminosulfonylamino)pentanoic acid methyl ester

https://huagongshe.com/reaction/743429

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(N-carbobenzyloxyaminosulfonyl)aminopentanoic acid methyl esterHCID 54269521—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-(Aminosulfonylamino)pentanoic acid methyl esterHCID 5391682576%

Reaction Steps

A solution of 2-(N-carbobenzyloxyaminosulfonyl) aminopentanoic acid methyl ester (33 g) in methanol (250 ml) under nitrogen was cooled to 0° C. and 1.4 g of 10% Pd/C was added. The mixture was placed into a Parr Apparatus and hydrogenated for 2 hours. The catalyst was removed on a pad of CELITE® and the filtrate was concentrated in vacuo and purified by flash silica gel chromatography (50% ethyl acetate in hexane) to afford 13.5 g (76%) of 2-(aminosulfonylamino)pentanoic acid methyl ester (Formula VII: R=CH3 ; R1 =H; R2 =propyl; R3 =H) as a solid, m.p. 63°-64° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556909
Source datasetuspto-grants-1996_09
ORD IDord-ac98cc0c86674778bc0cd3ae9b1cb50e
Source noteuspto-grants-1996_09