Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 68781601 | HCID 68781601 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58972439 | HCID 58972439 | 83% |
Reaction Steps
To a stirred solution of 4-[4-(2-hydroxy-ethylamino)-6-methoxy-[1,3,5]triazin-2-ylamino]-piperidine-1-carboxylic acid tert-butyl ester (1.00 g, 2.7 mmol, 1.0 equiv) in ethanol (30 mL) was added 4 M HCl in dioxane (3.40 mL, 13.6 mmol, 5.0 equiv) drop by drop. The reaction mixture was subsequently stirred at rt for 72 h and at 80° C. for 2 h. It was then cooled down to rt, poured into ice water and the pH was adjusted to 9-10 by addition of a sat. solution of potassium carbonate. The solution was extracted six times with a mixture of dichloromethane/isopropanol (4:1). The combined organic layers were concentrated by evaporation under reduced pressure to yield 0.60 g (83%) of the title compound as light yellow oil. MS (ISP): 269.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855194B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-5a8db8634f0545bd80bf84eacda0b24b |
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| Source note | uspto-grants-2010_12 |
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