Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 215797-69-6 | HCID 54592902 | — |
| Reactant | HCID 59263885 | HCID 59263885 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59263935 | HCID 59263935 | — |
Reaction Steps
Benzyl 2-(N-cyclohexylacrylamido)ethyl(2-(4-hydroxy-2-oxo-2,3-dihydrobenzo[d]thiazol-7-yl)ethyl)carbamate prepared as in Example 12 step i) (0.33 g), 2,3-difluorophenethylamine hydrochloride (0.244 g) and triethylamine (0.176 mL) were dissolved in ethanol (3 mL) and heated at 60° C. for 48 h. The mixture was cooled to room temperature, quenched with water, extracted with ethyl acetate, washed with water and brine, dried (Na2SO4), filtered and evaporated in vacuo to afford the sub-title product (0.420 g) as a light brown gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700782B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-5f7ec1aa75354a69a5358ffaacc86e72 |
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| Source note | uspto-grants-2010_04 |
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