HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(carbobenzyloxyaminosulfonyl)-2-piperidine-carboxylic acid methyl ester → N-(aminosulfonyl)-2-piperidinecarboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(carbobenzyloxyaminosulfonyl)-2-piperidine-carboxylic acid methyl ester | HCID 53700895 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(aminosulfonyl)-2-piperidinecarboxylic acid methyl ester | HCID 53861949 | 91.5% |
Reaction Steps
A solution of N-(carbobenzyloxyaminosulfonyl)-2-piperidine-carboxylic acid methyl ester (29.8 g) in methanol (300 ml) under nitrogen was cooled to 0° C. and 1.8 g of 10% Pd/C was added. The mixture was placed into a Parr Apparatus and hydrogenated for 2 hours at 55 psi. The catalyst was removed on a pad of CELITE® and the filtrate was concentrated in vacuo and purified by flash silica gel chromatography (35-40% ethyl acetate/hexane) to afford 17 g (90%) of N-(aminosulfonyl)-2-piperidinecarboxylic acid methyl ester (Formula VII: R=CH3 ; R1 =H; R2 and R3 together=--(CH2)4 --) as a solid, m.p. 72°-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05494925 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-e6e6750ba66c481d957418d1552c37b0 |
| Source note | uspto-grants-1996_02 |