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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965146Generated: October 31, 2026

Tetrahydrofuran → N4-Hydroxy-2-isobutyl-N1-(9-oxo-1,8-diaza-tricyclo(10.6.1.013,18)nonadeca-12(19),13,15,17-tetraen-10-YL)-succinamide

https://huagongshe.com/reaction/965146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant(3R,10S)-N-benzyloxy-5-methyl-3-(9-oxo-1,8-diazatricyclo[10.6. 1.013,18]nonadeca-12(19),13(18),14,16-tetraen-10-ylcarbamoyl)hexanamideHCID 86752868—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN4-Hydroxy-2-isobutyl-N1-(9-oxo-1,8-diaza-tricyclo(10.6.1.013,18)nonadeca-12(19),13,15,17-tetraen-10-YL)-succinamideHCID 47837992%

Reaction Steps

Alternatively, (3R,10S)-N-benzyloxy-5-methyl-3-(9-oxo-1,8-diazatricyclo[10.6.1.013,18 ]nonadeca-12(19),13(18),14,16-tetraen-10-ylcarbamoyl)hexanamide (1.0 g, 1.83 mmol) was taken up in a solution of 20% THF in ethanol (500 mL) and then Pd on activated charcoal (200 mg) was added portionwise. The resulting slurry was stirred as H2 gas was gently bubbled through the solution. After 4 hours, the reaction mixture was suction filtered through a bed of celite (1.5 cm), and the filtrate was concentrated and then taken up in methanol (30 mL) and filtered through a plug of cotton. Recrystallization from methanol/ethyl acetate/ether/petroleum ether gave (3R,10S)-N-hydroxy-5-methyl-3-(9-oxo-1,8-diazatricyclo[10.6.1.013,18 ]nonadeca-12(19),13(18),14,16-tetraen-10-yl-carbamoyl)hexanamide (768 mg, 92%), MS: 455 (M-H)-.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05773428
Source datasetuspto-grants-1998_06
ORD IDord-74099e9dc638401aa3db8c6109c11de7
Source noteuspto-grants-1998_06