HuagongsheHuagongshe Chemistry Print Report · For research reference only
(N-carbobenzyloxyaminosulfonyl)-2-(3-methylbutyl)sarcosine methyl ester → N-(aminosulfonyl)-2-(3-methylbutyl)sarcosine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (N-carbobenzyloxyaminosulfonyl)-2-(3-methylbutyl)sarcosine methyl ester | HCID 18922249 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(aminosulfonyl)-2-(3-methylbutyl)sarcosine methyl ester | HCID 18922252 | 98.7% |
Reaction Steps
A solution of (N-carbobenzyloxyaminosulfonyl)-2-(3-methylbutyl)sarcosine methyl ester (20.6 g, 53.17 mmol) in 200 ml of methanol under nitrogen was cooled to 0° C. and 1.5 g of 10% Pd/C was added. The mixture was placed on a Parr Apparatus at 50 psi and hydrogenated for 3.5 hours. The catalyst was removed on a pad of CELITE® and the filtrate was concentrated in vacuo to afford 13.24 g (98.6%) of N-(aminosulfonyl)-2-(3-methylbutyl)sarcosine methyl ester (Formula V: R=CH3 ; R1 =(CH2)2CH(CH3)2 ; R2 =H; R3 =CH3) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05750546 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-98de722c4f084b57a7a3336ab1853c10 |
| Source note | uspto-grants-1998_05 |