Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 131736717 | HCID 131736717 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 90047196 | HCID 90047196 | 87% |
Reaction Steps
(S)-tert-Butyl 2-(4-(1-(5-bromopyridin-2-yl)-1H-1,2,3-triazole-4-carboxamido)phenyl)morpholine-4-carboxylate (63 mg, 0.12 mmol) was dissolved in dioxane (0.5 ml) and a solution of HCl in dioxane (4 M, 0.36 ml, 1.44 mmol) was added. The reaction mixture was stirred for 2 hours at 60° C. After cooling, ether was added, the solid was filtered off, washed with ether and dried in vacuo at 60° C. to afford (S)-1-(5-bromopyridin-2-yl)-N-(4-(morpholin-2-yl)phenyl)-1H-1,2,3-triazole-4-carboxamide hydrochloride (48 mg, 87%) as a white solid. MS (ISP): 429.4 ({79Br} [M−H]+), 431.5 ({81Br} [M−H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09416127B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-c4c4a3de6b4740cc858ddc7c17851f7d |
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| Source note | uspto-grants-2016_08 |
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