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| | 4-Amino-2-methyl-10H-thiene[2,3-b][1,5]benzodiazepine hydrochloride Basic information | | Synthesis |
| | 4-Amino-2-methyl-10H-thiene[2,3-b][1,5]benzodiazepine hydrochloride Chemical Properties |
| Melting point | 283-285°C | | storage temp. | Keep in dark place,Inert atmosphere,Store in freezer, under -20°C | | solubility | DMSO (Slightly), Methanol (Sparingly, Sonicated) | | form | Solid | | color | Yellow to Dark Beige | | InChI | InChI=1S/C12H11N3S.ClH/c1-7-6-8-11(13)14-9-4-2-3-5-10(9)15-12(8)16-7;/h2-6,15H,1H3,(H2,13,14);1H | | InChIKey | FDWMAKNNNPSUTL-UHFFFAOYSA-N | | SMILES | C12SC(C)=CC=1C(N)=NC1=CC=CC=C1N2.Cl | | CAS DataBase Reference | 138564-60-0(CAS DataBase Reference) |
| | 4-Amino-2-methyl-10H-thiene[2,3-b][1,5]benzodiazepine hydrochloride Usage And Synthesis |
| Synthesis | In a 500 mL round-bottom flask equipped with a mechanical stirrer and thermometer, 10.0 g (0.0386 mol) of 5-methyl-2-((2-nitrobenzene)amino)thiophene-3-carboxynitrile (1) and 100 mL of ethanol were added. Then 7.4 g (0.062 mol) of tin powder and 84 mL of 4M hydrochloric acid were added, and the mixture was stirred at 50 °C for 0.5 h. The temperature of the reaction mixture was raised to 85 °C, and stirring was continued for 4 h. The mixture was then cooled to 25 °C and stirred for another 8 h, which resulted in the precipitation of a solid. The precipitated crystals were collected, washed with 20 mL of ethanol, and dried under vacuum. 9.8 g (96%) of 2-methyl-2-(nitrobenzene) ... ![Synthetic route of 4-Amino-2-methyl-10H-thiene[2,3-b][1,5]benzodiazepine hydrochloride Synthetic route of 4-Amino-2-methyl-10H-thiene[2,3-b][1,5]benzodiazepine hydrochloride](https://www.chemicalbook.com/NewsImg/2022-10-08/6380081821409211462375084.jpg)
| | Chemical Properties | Yellow Crystaline solid | | Uses | Intermediate in the preparation of Olanzapine (O253750). |
| | 4-Amino-2-methyl-10H-thiene[2,3-b][1,5]benzodiazepine hydrochloride Preparation Products And Raw materials |
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