1,4-Dioxane hydrochloride → 1622993-13-8
Reaction equation
[ClH:1].O1CCOCC1.[Br:8][C:9]1[N:25]=[C:12]2[CH:13]=[C:14]([NH:17]C(=O)OC(C)(C)C)[CH:15]=[CH:16][N:11]2[N:10]=1>O1CCOCC1>[ClH:1].[Br:8][C:9]1[N:25]=[C:12]2[CH:13]=[C:14]([NH2:17])[CH:15]=[CH:16][N:11]2[N:10]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A suspension of 4 N hydrochloric acid-1,4-dioxane (8 ml) and 1,4-dioxane (8 ml) containing the tert-butyl (2-bromo-[1,2,4]triazolo[1,5-a]pyridin-7-yl)carbamate (400 mg) obtained in (Example 3.15) <Step 4> was heated to reflux for 40 minutes. Thereafter, the precipitated solid was collected by filtration, and was then washed with 1,4-dioxane (15 ml). The obtained solid was dried to obtain the title compound (279 mg) in the form of a white solid.
Workup
- customobtained in (Example 3.15) <Step 4>
- temperaturewas heated
- temperatureto reflux for 40 minutes
- filtrationThereafter, the precipitated solid was collected by filtration
- washwas then washed with 1,4-dioxane (15 ml)
- customThe obtained solid was dried
Sources & evidence
- ORD record
- ord-fb9c287d09eb47e798457aaefe96e7f6
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09440970B2
Reaction notes
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