HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931380Generated: October 31, 2026
Diisopropylethylamine → HCID 67434519, compound
https://huagongshe.com/reaction/931380
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-((2-(Trimethylsilyl)ethoxy)methyl)-1,3-dihydro-2H-pyrrolo(2,3-b)pyridin-2-one | HCID 57458886 | — |
| Reactant | HCID 58458881 | HCID 58458881 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67434519 | HCID 67434519 | — |
Reaction Steps
N,N-Diisopropylethylamine (3.64 mL, 22 mmol) is added to a stirred solution of 1-{[2-(trimethylsilyl)ethoxy]methyl}-1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one (prepared according to the procedures described in WO2008/020902) (2.64 g, 10 mmol) in THF (75 mL) at ambient temperature. To the stirred mixture is added dropwise a solution of 2-(bromomethyl)-5-nitrobenzoyl chloride (3.06 g, 11 mmol) [Pifferi et al. (1966) Tetrahedron 22, 2107] in THF (75 mL) and the mixture is then stirred at ambient temperature for 18 h. The mixture is then partitioned between EtOAc and saturated aqueous NaHCO3. The layers are separated and the aqueous layer further extracted with EtOAc. The combined organic extracts are washed with brine, dried (Na2SO4) and concentrated in vacuo. The residue is purified by silica gel chromatography (gradient elution with hexanes-EtOAc) to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296750B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-292779559f674d01b9fd7c21c7777586 |
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| Source note | uspto-grants-2016_03 |
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