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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766842Generated: November 2, 2026

2,4-Dimethylbenzaldehyde → HCID 11454345, compound

https://huagongshe.com/reaction/1766842

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DimethylbenzaldehydeHCID 61814—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 69287829HCID 69287829—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 11454345HCID 11454345—

Reaction Steps

A solution of {(25, 3S)-2-[2-(5-tert-butyl-[1,3,4]thiadiazol-2-ylcarbamoyl)-acetylamino]-3-hydroxy-hex-4-ynyl}-carbamic acid benzyl ester (90 mg, 0.19 mmol) in MeOH (4 mL) was charged with 5% Pd/C, Degussa style (18 mg), stirred under H2 (1 atm) for 12 h at RT, filtered, and concentrated in vacuo. The residue was dissolved in MeOH (3 mL). The resultant solution was charged sequentially with 2,4-dimethylbenzaldehyde (0.02 mL, 0.14 mmol) and sodium cyanoborohydride (11 mg, 0.18 mmol), stirred for 12 h at RT, quenched with sat. NaHCO3, and extracted twice with EtOAc. The organic extracts were combined, washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo. Purification of the residue by reverse-phase HPLC provided the title compound as a white powder after lyopholization. MS found: (M+H)+=476.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230133B2
Source datasetuspto-grants-2007_06
ORD IDord-c541d18bc849442585728e08468761f7
Source noteuspto-grants-2007_06