HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766833Generated: October 31, 2026
Propanal → N-{(1S,2S)-1-[(2,4-Dimethyl-benzylamino)-methyl]-2-hydroxy-pentyl}-N'-(3-propylamino-5-trifluoromethyl-phenyl)-malonamide
https://huagongshe.com/reaction/1766833
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propanal | HCID 527 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | {(2S,3S)-2-[2-(3-amino-5-trifluoromethyl-phenylcarbamoyl)-acetylamino]-3-hydroxyhexyl}-(2,4-dimethyl-benzyl)-carbamic acid benzyl ester | HCID 68616642 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-{(1S,2S)-1-[(2,4-Dimethyl-benzylamino)-methyl]-2-hydroxy-pentyl}-N'-(3-propylamino-5-trifluoromethyl-phenyl)-malonamide | HCID 11226430 | — |
Reaction Steps
A solution of {(2S,3S)-2-[2-(3-amino-5-trifluoromethyl-phenylcarbamoyl)-acetylamino]-3-hydroxyhexyl}-(2,4-dimethyl-benzyl)-carbamic acid benzyl ester (97 mg, 0.15 mmol) in MeOH (3 mL) was charged with propionaldehyde (0.01 mL, 0.15 mmol), stirred for 15 min at RT, and then charged with sodium cyanoborohydride (12 mg, 0.19 mmol). The reaction was stirred at RT for 12 h, concentrated in vacuo, and dissolved in EtOAc. The resultant solution was washed successively with water, sat. NaHCO3, water, and brine. The organic phase was dried (Na2SO4), filtered, and concentrated in vacuo. The residue was dissolved in MeOH (3 mL). This solution was charged with 5% Pd/C, Degussa style (11 mg), stirred under H2 (1 atm) for 12 h at RT, 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)+=537.4.
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-9681aa0ef279433b96d985ed3ea9229a |
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| Source note | uspto-grants-2007_06 |
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