HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391606Generated: October 29, 2026
Diisopropylethylamine → HCID 57657815, compound
https://huagongshe.com/reaction/391606
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Bromonicotinic acid | HCID 88707 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 57657850 | HCID 57657850 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57657815 | HCID 57657815 | — |
Reaction Steps
To the solution of (S)-Methyl 5-(S-phenylsulfonimidoyl)pentanoate (475 mg, 1.86 mmol) in anhydrous DMF (6 mL) at room temperature under nitrogen atmosphere was added diisopropylethylamine (0.65 mL), 5-bromonicotinic acid (0.38 g), and (benzotriazol-1-yloxy)-tris(dimethylamino)-phosphonium hexafluorophosphate (0.81 g). The resulting reaction mixture was stirred for about 15 min at room temperature and then poured into saturated aqueous NaHCO3. The aqueous was extracted with EtOAc (1×), which was then washed with saturated aqueous NaHCO3 and brine (v:v 1:1, 2×), brine (1×), and dried with anhydrous sodium sulfate. The solution was decanted and concentrated with silica gel. A column chromatography (EtOAc-Hex 1:2) rendered the title compound as slightly yellow colored solid in amount of (616 mg, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383825B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-2da21dd3b36c4574bd69dd5ac484d5f3 |
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| Source note | uspto-grants-2013_02 |
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