HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536213Generated: October 28, 2026
Ethylenediamine → 3-(benzyloxy)-6-(4,5-dihydro-1H-imidazol-2-yl)-2-methoxyaniline
https://huagongshe.com/reaction/536213
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Reactant | 2-Amino-4-(benzyloxy)-3-methoxybenzonitrile | HCID 58219849 | — |
| Product | 3-(benzyloxy)-6-(4,5-dihydro-1H-imidazol-2-yl)-2-methoxyaniline | HCID 7059268 | 86% |
Reaction Steps
A mixture of 2-amino-4-(benzyloxy)-3-methoxybenzonitrile (Step 5, 144 g, 566 mmol) and sulfur (55 g, 1.7 mol) in ethylenediamine (800 mL) was degassed for 30 minutes then heated to 100° C. After 16 h the reaction mixture was cooled to room temperature and then filtered. The filtrate was concentrated under reduced pressure, diluted with a saturated sodium bicarbonate solution and extracted with EtOAc. The organic layer was washed with brine, dried (sodium sulfate), filtered and concentrated under reduced pressure. The resulting solids were recrystallized from EtOAc and hexanes to afford the title compound (145 g, 86%): 1H NMR (DMSO-d6) δ: 7.27-7.48 (5H, m), 7.14 (1H, d), 6.92 (2H, m), 6.64 (1H, m), 6.32 (1H, d), 5.11 (2H, s), 3.67 (3H, s), 3.33 (2H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859572B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-c6c6afeffd70414688a1d38d563bbe29 |
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| Source note | uspto-grants-2014_10 |
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