HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → ((2S)-2-amino-3-methylbutyl)carbamic acid p-nitrobenzyl ester hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | ((2S)-2-t-butoxycarbonylamino-3-methylbutyl)carbamic acid p-nitrobenzyl ester | HCID 69544030 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | ((2S)-2-amino-3-methylbutyl)carbamic acid p-nitrobenzyl ester hydrochloride | HCID 69544240 | 70% |
Reaction Steps
To a solution of ((2S)-2-t-butoxycarbonylamino-3-methylbutyl)-carbamic acid p-nitrobenzyl ester (3.13 g, 8.21 mmol) (obtained as described in Reference Example 61(3)) in 1,4-dioxane (31 ml) was added a 4N solution of hydrogen chloride in 1,4-dioxane (31 ml) in an ice bath, and the mixture was stirred at room temperature for 4 hours. After checking the completion of the reaction, the reaction mixture was concentrated under reduced pressure. Ethyl acetate was added to the residue, and the resulting mixture was filtered off and washed with ethyl acetate to give ((2S)-2-amino-3-methylbutyl)carbamic acid p-nitrobenzyl ester hydrochloride (1.82 g, yield 70%) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07001897B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-58203e05c0824c04a2f5576a5da5ae0f |
| Source note | uspto-grants-2006_02 |