HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419337Generated: October 29, 2026
Dimethylamine → 4-{5-[(Dimethylamino)methyl]-1,3,4-oxadiazol-2-yl}-2-(methyloxy)aniline
https://huagongshe.com/reaction/419337
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(Chloromethyl)-5-[3-(methyloxy)-4-nitrophenyl]-1,3,4-oxadiazole | HCID 59452661 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-{5-[(Dimethylamino)methyl]-1,3,4-oxadiazol-2-yl}-2-(methyloxy)aniline | HCID 59452910 | 89.2% |
Reaction Steps
To 2-(chloromethyl)-5-[3-(methyloxy)-4-nitrophenyl]-1,3,4-oxadiazole (0.399 g, 1.48 mmol) in dioxane (10 mL) was added dimethylamine (1.87 mL, 40% weight in H2O, 14.8 mmol). The reaction was heated at 60° C. overnight. The reaction was poured into half saturated NaHCO3, extracted with DCM and EtOAc, dried (MgSO4) and concentrated. The residue was taken up in EtOAc (20 mL) and Pd on carbon was added in one portion. The mixture was stirred at rt under H2 (1 atm.) until complete by TLC. The reaction was filtered through Celite® and concentrated to provide the title compound of step D (0.326 g, 1.32 mmol, 89% over two steps). 1H NMR (400 MHz, DMSO-d6) δ ppm 2.18-2.23 (m, 6H), 3.67-3.72 (m, 2H), 3.76-3.82 (m, 3H), 5.47-5.56 (m, 2H), 6.64-6.72 (m, 1H), 7.25 (d, J=2.0 Hz, 1H), 7.30 (dt, J=8.1, 2.1 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093239B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-32accc09dc514616b7a46a271dd2feb4 |
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| Source note | uspto-grants-2012_01 |
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