HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341253Generated: October 31, 2026
Dicyclohexylcarbodiimide → N-[(1S)-1-benzyl-2-hydroxyethyl]-4-pyridin-4-ylbenzamide
https://huagongshe.com/reaction/341253
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | phenylalaninol, (S)- | HCID 447213 | — |
| Reactant | 4-(Pyridin-4-yl)benzoic acid | HCID 1520811 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | N-[(1S)-1-benzyl-2-hydroxyethyl]-4-pyridin-4-ylbenzamide | HCID 68513305 | — |
Reaction Steps
In a microwave vial containing 3 eq. of PS-DCC, 4-(pyridin-4-yl)benzoic acid (20 mg, 0.1 mmol) was added dissolved in DMA (1.0 ml). Then a solution of HOBT (14 mg, 0.1 mmol) dissolved in DMA (0.3 ml) was added followed by the addition of DIEA (36 μl, 0.2 mmol) dissolved in DMA (0.3 ml) and the addition of (S)-2-amino-3-phenylpropan-1-ol (17 mg, 0.11 mmol) dissolved in DMA (0.6 ml). The mixture was heated in the microwave to 100° C. for 600 seconds. The reaction was filtered through Si-Carbonate, 6 ml-1 g supplied by Silicycle chemical Division and transferred to 20 ml vials. The reaction was checked by LC/MS and concentrated to dryness. The residues were dissolved in 1:1 DMSO/MeOH and purified by reverse phase HPLC (TFA method). Product was characterized by 1H NMR, MS and LC/MS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895749B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-ffec783dbdbf47d7a5abb5b90d983cbc |
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| Source note | uspto-grants-2014_11 |
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