HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl[(1S)-2-({3-[(tert-butoxycarbonyl)amino]-2-hydroxypropyl}amino)-1-(hydroxymethyl)-2-oxoethyl]carbamate → N-{3-[(tert-Butoxycarbonyl)amino]-2-hydroxypropyl}-L-serinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl[(1S)-2-({3-[(tert-butoxycarbonyl)amino]-2-hydroxypropyl}amino)-1-(hydroxymethyl)-2-oxoethyl]carbamate | HCID 131727151 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-{3-[(tert-Butoxycarbonyl)amino]-2-hydroxypropyl}-L-serinamide | HCID 86619427 | — |
Reaction Steps
131 mg (0.318 mmol) of benzyl[(1S)-2-({3-[(tert-butoxycarbonyl)amino]-2-hydroxypropyl}amino)-1-(hydroxymethyl)-2-oxoethyl]carbamate (Example 100A) are dissolved in 20 ml of ethanol. 20 mg of palladium on activated carbon (10%) are added thereto, and the mixture is hydrogenated under atmospheric pressure for 15 h. The reaction mixture is filtered through prewashed kieselguhr, and the filtrate is concentrated in vacuo on a rotary evaporator. The crude product is reacted without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07446102B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-cf54cee1f4db40239d57e0ac1d8884b1 |
| Source note | uspto-grants-2008_11 |