HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631045Generated: November 2, 2026
Diisopropylethylamine → HCID 86660285, compound
https://huagongshe.com/reaction/1631045
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 86660283 | HCID 86660283 | — |
| Solvent | Dichloromethane ethanol | HCID 21584144 | — |
| Product | HCID 86660285 | HCID 86660285 | 101.4% |
Reaction Steps
A solution of methyl (2S,4R)-4-(tert-butyldimethylsilyloxy)-1-(3-chloro-5-cyanopyridin-2-yl)pyrrolidine-2-carboxylate (0.306 g; 0.77 mmol), hydroxylamine hydrochloride (0.064 g; 0.92 mmol) and DIEA (0.176 mL; 1.01 mmol) in EtOH/DCM (4 mL/2 mL) was stirred at ambient temperature for 96 hours. The solvent was evaporated in vacuo and the residue dissolved in DCM/water. The mixture was passed through a hydrophobic frit and the solvent evaporated in vacuo to afford the title product (0.335 g, 100%). 1H NMR (CDCl3, 400 MHz) δ 8.22 (1H, d, J=2 Hz), 7.76 (1H, d, J=1.6 Hz), 6.60 (1H, br s), 4.87-4.83 (1H, m), 4.73 (2H, br s), 4.54-4.53 (1H, m), 4.26-4.22 (1H, m), 3.75-3.67 (4H, m), 2.26-2.20 (1H, m), 2.09-2.02 (1H, m), 0.85 (9H, s), 0.05-0.08 (6H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791142B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-6f123790efd34d64910bb62865f79aa7 |
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| Source note | uspto-grants-2014_07 |
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