HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(N-carbobenzyloxyaminosulfonyl)aminopentanoic acid methyl ester → 2-(Aminosulfonylamino)pentanoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(N-carbobenzyloxyaminosulfonyl)aminopentanoic acid methyl ester | HCID 54269521 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(Aminosulfonylamino)pentanoic acid methyl ester | HCID 53916825 | 67.5% |
Reaction Steps
A solution of 2- (N-carbobenzyloxyaminosulfonyl) aminopentanoic acid methyl ester (26.7 g) in methanol (200 ml) under nitrogen was cooled to 0° C. and 1.5 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 (4-6% methanol in methylene chloride) to afford 11.0 g (62%) 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05494925 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-9009730ba5cd4b22aa9accbfa523e32d |
| Source note | uspto-grants-1996_02 |