HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638096Generated: October 30, 2026
Water → 7-[(1-[2(R)-((1,1-dimethylethoxy)carbonyl)amino-4-methylpentanoyl]-2,3-dihydro-1H-indol-3-yl)methyl]quinazolino(3,2-A)-1,4-benzodiazepin-5,13-(5H,7H)-dione hydrate
https://huagongshe.com/reaction/638096
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 7-[(1-[2(R)-((1,1-Dimethylethoxy)carbonyl)amino-4-methylpentanoyl]-2,3-dihydro-1H-indol-3-yl)methyl]quinazolino(3,2-A)-1,4-benzodiazepin-5,13-(6H,7H)-dione | HCID 54535365 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 7-[(1-[2(R)-((1,1-dimethylethoxy)carbonyl)amino-4-methylpentanoyl]-2,3-dihydro-1H-indol-3-yl)methyl]quinazolino(3,2-A)-1,4-benzodiazepin-5,13-(5H,7H)-dione hydrate | HCID 70479951 | — |
Reaction Steps
7-[(1-[2(R)-((1,1-dimethylethoxy)carbonyl)amino-4-methylpentanoyl]-2,3-dihydro-1H-indol-3-yl)methyl]quinazolino(3,2-A)-1,4-benzodiazepin-5,13-(6H,7H)-dione (120 mg, 0.19 mmole) was dissolved in 3 ml of glacial acetic acid and treated at 10° with 48 mg (0.77 mmole) of sodium cyanoborohydride. After twenty minutes, the reaction mixture was poured into 50 ml of water, extracted with ethyl acetate (4×40 ml) and the combined organic extracts were washed with saturated sodium bicarbonate solution and brine, then dried (MgSO4) and concentrated. The crude product was purified by preparative thick layer chromatography on silica gel (98:2 chloroform-methanol, multiple elutions) to give the analytical product as isomer 2, the slower eluting component.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04559339 |
|---|
| Source dataset | uspto-grants-1985_12 |
|---|
| ORD ID | ord-c0f6b8fc0d1f4e26b7b1e35a6b316831 |
|---|
| Source note | uspto-grants-1985_12 |
|---|