1,4-Dioxane hydrochloride → HCID 90308838, compound
Reaction equation
[ClH:1].O1CCOCC1.C(OC(=O)[NH:14][C:15]1[CH:19]=[C:18]([C:20]2[N:25]=[CH:24][CH:23]=[CH:22][N:21]=2)[S:17][CH:16]=1)(C)(C)C>>[ClH:1].[N:21]1[CH:22]=[CH:23][CH:24]=[N:25][C:20]=1[C:18]1[S:17][CH:16]=[C:15]([NH2:14])[CH:19]=1Participants
3
Procedure
A 4 N hydrochloric acid-dioxane solution (8 mL) was added to tert-butyl(5-(pyrimidin-2-yl)thiophen-3-yl)carbamate obtained in the above-described Step (544 mg), and the reaction solution was stirred at room temperature for 90 minutes. The solvent was evaporated under vacuum to obtain 5-(pyrimidin-2-yl)thiophen-3-amine hydrochloride as a brown solid.
Workup
- customobtained in the above-described Step (544 mg)
- customThe solvent was evaporated under vacuum
Sources & evidence
- ORD record
- ord-aec8e9d4b366408eb44b3c8bf685e0a6
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09145414B2
Reaction notes
Loading…