HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236193Generated: November 3, 2026
Diisopropylethylamine → HCID 59301328, compound
https://huagongshe.com/reaction/2236193
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (2-Methoxyethyl)(methyl)amine | HCID 300977 | — |
| Reactant | 5-Bromo-2-nitropyridine | HCID 817620 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59301328 | HCID 59301328 | 41% |
Reaction Steps
A solution of 2-nitro-5-bromopyridine (500 mg, 3.15 mmol) in EtOH (15 mL) was treated with methoxyethyl-N-methylamine (1.12 g, 12.6 mmol) and diisopropylethylamine (2.2 mL, 12.6 mmol). The resulting mixture was then heated in a sealed tube at 90° C. for 4 days then cooled and partitioned between EtOAc and water. The organic layer was dried over Na2SO4, filtered and concentrated. The residue was chromatographed on a silica gel column with a 40-100% EtOAc in hexanes gradient to afford the product as a thick yellow oil that crystallized slowly upon standing (270 mg, 41% yield). HRMS m/z calcd for C9H13N3O3 [M+Na]+: 234.0849; Found: 234.0850.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07714126B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-2d952bd451d7492c899da99e014a52de |
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| Source note | uspto-grants-2010_05 |
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