HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766842Generated: November 2, 2026
2,4-Dimethylbenzaldehyde → HCID 11454345, compound
https://huagongshe.com/reaction/1766842
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dimethylbenzaldehyde | HCID 61814 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 69287829 | HCID 69287829 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11454345 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07230133B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-c541d18bc849442585728e08468761f7 |
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| Source note | uspto-grants-2007_06 |
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