Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethanolamine | HCID 7618 | — |
| Reactant | 1H-Imidazole-1-propanamine | HCID 78736 | — |
| Reactant | 5-Fluoro-2-nitrotoluene | HCID 94956 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 11514448 | HCID 11514448 | — |
Reaction Steps
150 ml of dimethyl sulfoxide were introduced into a 500 ml three-necked flask and treated with 22.6 g of triethanolamine (99% strength), 28.7 g of 1-(3-amino-propyl)imidazole (98% strength) and 24.2 g of 5-fluoro-2-nitrotoluene (96% strength). The mixture was stirred at 80° C. for 17 h. Following this, the batch was cooled to room temperature and poured onto 1 l of ice, a yellow oil depositing, which crystallized thoroughly after about 1 h. The precipitate thus resulting was filtered off with suction, washed with water and dried in vacuo at 40° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07081140B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-6c83fa214378440c89210958526a08e4 |
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| Source note | uspto-grants-2006_07 |
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