HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987175Generated: October 31, 2026
Diisopropylethylamine → HCID 44249374, compound
https://huagongshe.com/reaction/1987175
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Bis(2-oxo-3-oxazolidinyl)phosphinic chloride | HCID 152842 | — |
| Reactant | 1-(4-Amino-3-fluorophenyl)pyridin-2-one | HCID 22181548 | — |
| Reactant | HCID 34180170 | HCID 34180170 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 44249374 | HCID 44249374 | — |
Reaction Steps
Compound 7a (1.85 g; 6 mmol) is suspended in acetonitrile (20 ml) and N,N-diisopropyl ethyl amin (1.65 ml; 10 mmol) is added at 25° C. BOP-CL (2.46 g; 10 mmol) is added as a solid and after stirring for 30 min at 25° C. 1-(4-amino-3-fluoro-phenyl)-1H-pyridin-2-one (1.45 g; 7 mmol) is added to the reaction mixture. The mixture is stirred for 4 d at 25° C., evaporated to dryness and dissolved in ethyl acetate (200 ml). The organic phase is washed with 2 N HCl (50 ml), with 10% aqueous Na2CO3 solution, water and brine and dried over Na2SO4. The organic phase is filtered and the filtrate is evaporated to dryness. The crude product is purified by silica gel chromatography. Yield: 1.77 g (58.1%), ESI-MS: m/z=472 [M−H]−
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07550487B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-96509bd7381d43a3a521aa219c227dde |
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| Source note | uspto-grants-2009_06 |
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