Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 18956296 | HCID 18956296 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18956279 | HCID 18956279 | 31.6% |
Reaction Steps
A mixture of 2-(diaminomethyleneamino)-4-[6-(1-tert-butoxycarbonylpiperidin-3-yl)carbonylaminomethylpyridin-2-yl]thiazole (1.9 g) and 4N-methanolic hydrogen chloride (40 ml) was stirred for 7 hours at ambient temperature. To the reaction mixture was added a tetrahydrofuran (40 ml) and the isolated precipitate was collected by filtration. The precipitate was added to water and adjusted to pH 13 with 5N-sodium hydroxide. The mixture was extracted with a mixture of ethyl acetate and tetrahydrofuran. The extract was washed with brine, dried over magnesium sulfate and evaporated in vacuo. The residue was recrystallized from a mixture of methanol, dioxane and diisopropyl ether to give 2-(diaminomethyleneamino)-4-[6-(3-piperidyl)carbonylaminomethylpyridin-2-yl]thiazole (0.47 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05364871 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-72f2bf314475498cae3ae0f097c7aeb4 |
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| Source note | uspto-grants-1994_11 |
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