HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → (S)-tert-butoxycarbonylamino-3-thiocarbamoyl-propionic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | Benzyl N~2~-(tert-butoxycarbonyl)-L-asparaginate | HCID 14420402 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-tert-butoxycarbonylamino-3-thiocarbamoyl-propionic acid benzyl ester | HCID 86654757 | — |
Reaction Steps
A 1-L round bottom flask was charged with (S)-benzyl 4-amino-2-(tert-butoxycarbonylamino)-4-oxobutanoate (10.0 g, 31.0 mmol), Lawesson's reagent (6.58 g, 16.3 mmol), and tetrahydrofuran (155 mL). Hydrazine (7.8 mL, 0.248 mol) was added and the resulting mixture was stirred at room temperature for 72 h. The resulting mixture was then concentrated in vacuo and the residue purified via flash silica gel chromatography (Analogix IF-280, SF40-400 g column, gradient 90:10-60:40 Heptane:EtOAc) to yield-(S)-tert-butoxycarbonylamino-3-thiocarbamoyl-propionic acid benzyl ester. MS (ES+) 339 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552032B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-3543d5515422496ba01160057b056898 |
| Source note | uspto-grants-2013_10 |