Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844318Generated: November 3, 2026

HCID 86654421, compound → HCID 86654422, compound

https://huagongshe.com/reaction/1844318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86654421HCID 86654421—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
CatalystPlatinumHCID 23939—
SolventAcetic AcidHCID 176—
ProductHCID 86654422HCID 86654422103%

Reaction Steps

A mixture of 2.62 g (4.86 mmol) of 3-[{(1S,4R)-4-[1-(acetyloxy)cyclobutyl]-4-[(benzyloxy)carbonyl]cyclopent-2-en-1-yl}(trifluoroacetyl)amino]-1,5-anhydro-2,3-dideoxy-4-O-methyl-D-erythro-pentitol and 750 mg each of 5% Pt/C and 5% Pd/C in 10 mL of acetic acid was stirred rapidly under 50 psi hydrogen gas for 18 h, then filtered through diatomaceous earth to remove catalyst. The filtrate was concentrated under reduced pressure, with added toluene to azeotropically remove acetic acid, to provide 2.25 g (103%) of the title compound as a white foam. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.50-1.71 (m, 3H) 1.74-1.84 (m, 1H) 2.02 (s, 3H) 2.04-2.17 (m, 1H) 2.34-2.55 (m, 5H) 2.60 (dd, J=14.3, 8.5 Hz, 1H) 2.66-2.81 (m, 2H) 3.30 (d, J=13.0 Hz, 1H) 3.35-3.39 (m, 1H) 3.42 (s, 3H) 3.47-3.56 (m, 1H) 3.83-3.91 (m, 1H) 4.13 (dd, J=11.6, 4.4 Hz, 1H) 4.16-4.23 (m, 1H) 4.26-4.38 (m, 1H). LC-MS ES+452.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946413B2
Source datasetuspto-grants-2015_02
ORD IDord-e7148dc31f794e5fb8ba556426ac8139
Source noteuspto-grants-2015_02