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 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05556909 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-ac98cc0c86674778bc0cd3ae9b1cb50e |
| Source note | uspto-grants-1996_09 |