HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482739Generated: October 29, 2026
Sodium borohydride → HCID 13604465, compound
https://huagongshe.com/reaction/482739
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13243522 | HCID 13243522 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13604465 | HCID 13604465 | — |
Reaction Steps
A solution of 3-(S)-t-butyloxycarbonylamino-1-ethoxycarbonylmethyl-2,3,4,5-tetrahydro-1H-[1]benzazepin-2,5-dione (0.14 g) and sodium borohydride (7 mg) in ethanol (10 ml) was stirred at room temperature for 18 hours. The ethanol was removed under reduced pressure, and the residue dissolved in dichloromethane (25 ml). The solution was extracted with 2N HCl (2×20 ml) and saturated brine (20 ml), and dried over sodium sulfate. The solvent was removed under reduced pressure, and the residue triturated with ether to give 3-(S)-t-butyloxycarbonylamino-1-ethoxycarbonylmethyl-5-hydroxy-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one, mp 167°-169.5° C., [α]D =-193° (c=0.52 in DMF). The substance was also obtained by hydrogenation of the benzazepin-2,5-dione derivative with H2 /Pt in ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04575503 |
|---|
| Source dataset | uspto-grants-1986_03 |
|---|
| ORD ID | ord-77724f358f1443a994a2b51c090f4c54 |
|---|
| Source note | uspto-grants-1986_03 |
|---|