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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant7-[(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)-dioneHCID 54535365—
SolventAcetic AcidHCID 176—
Product7-[(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 hydrateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04559339
Source datasetuspto-grants-1985_12
ORD IDord-c0f6b8fc0d1f4e26b7b1e35a6b316831
Source noteuspto-grants-1985_12