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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866522Generated: October 31, 2026

HCID 57978218, compound → HCID 57978258, compound

https://huagongshe.com/reaction/1866522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57978218HCID 57978218—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductAmmoniaHCID 222—
ProductHCID 57978258HCID 57978258187.4%

Reaction Steps

A suspension of methyl 3-[(2R)-2-({(2R)-2-[4-(benzyloxy)-3-(hydroxymethyl)phenyl]-2-hydroxyethyl}amino)propyl]benzoate (Preparation 61) (6.83 g, 15.2 mmol) and 10% palladium on carbon (683 mg) in ethanol (100 ml) was stirred under an atmosphere of hydrogen (60 psi) at room temperature for 18 hours. The catalyst was filtered off through arbocel and the filtrate concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with dichloromethane:methanol:880 ammonia (95:5:0.5 changing to 90:10:1, by volume) to give the title compound as a pale yellow gum (5.12 g). 1H NMR (400 MHz, CD3OD): δ=7.85-7.83 (1H, m), 7.79 (1H, s), 7.36-7.35 (2H, m), 7.20 (1H, s), 7.02-6.99 (1H, dd), 6.68-6.65 (1H, d), 4.61-4.58 (1H, m), 4.60 (2H, s), 3.90 (3H, s), 2.97-2.87 (2H, m), 2.80-2.62 (3H, m), 1.08-1.07 (3H, d) ppm. LRMS (electrospray): m/z [M+H]+ 360, [M+Na]+ 382, [M−H]− 358.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629358B2
Source datasetuspto-grants-2009_12
ORD IDord-41620a75b96a446592addd6db198a5d9
Source noteuspto-grants-2009_12