1,4-Dioxane hydrochloride → HCID 90309404, compound
Reaction equation
C(OC(=O)[NH:7][C:8]1[S:9][CH:10]=[C:11]([C:13]2[N:18]=[CH:17][CH:16]=[CH:15][N:14]=2)[CH:12]=1)(C)(C)C.[ClH:20].O1CCOCC1>>[ClH:20].[N:14]1[CH:15]=[CH:16][CH:17]=[N:18][C:13]=1[C:11]1[CH:12]=[C:8]([NH2:7])[S:9][CH:10]=1Participants
3
Procedure
A 4 N hydrochloric acid-dioxane solution (20 mL) was added to tert-butyl(4-(pyrimidin-2-yl)thiophen-2-yl)carbamate obtained in the above-described Step 3, and the reaction solution was stirred at room temperature for 2 hours. The solvent was evaporated under vacuum, and then isopropyl ether was added. The deposited precipitate was filtrated to obtain 4-(pyrimidin-2-yl)thiophen-2-amine hydrochloride.
Workup
- customobtained in the above-described Step 3
- customThe solvent was evaporated under vacuum
- additionisopropyl ether was added
- filtrationThe deposited precipitate was filtrated
Sources & evidence
- ORD record
- ord-b84e013cd56f45cc86b02ca6b52a50b6
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09145414B2
Reaction notes
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