HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239854Generated: November 2, 2026
Diisopropylethylamine → HCID 86648144, compound
https://huagongshe.com/reaction/239854
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 68776901 | HCID 68776901 | — |
| Reactant | HCID 86609688 | HCID 86609688 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86648144 | HCID 86648144 | — |
Reaction Steps
(2S)-2-{[(1S)-1-(4-bromophenyl)-2,2,2-trifluoroethyl]amino}-4,4-dichlorobutanoic acid (120 mg) and (1S)-1-cyano-2-(4-cyano-2-fluorophenyl)ethanaminium chloride (66 mg) were dissolved in DMF (1.5 ml) and HATU (223 mg) was added. The reaction mixture was stirred at room temperature for 5 min and Hunig's base (204 μL) was added. The solution was stirred for 18 hours. The mixture was poured onto an aqueous sodium hydrogen carbonate (saturated, 20 ml) and water (20 ml). The mixture was stirred in an erlenmeyer flask for 10 min. The aqueous layer was extracted with EtOAc. The organic layer was washed with brine, dried on MgSO4. It was concentrated under reduced pressure. The crude product was purified by flash (eluted with 20:80 to 55:45 EtOAc/hexanes).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642799B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-3dc1282e13904d98b863efcd6ece4b32 |
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| Source note | uspto-grants-2014_02 |
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