Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 10H-Thieno[2,3-b][1,5]benzodiazepin-4-amine, 2-methyl-, hydrochloride (1:1) | HCID 135525650 | — |
| Solvent | 1-Methylpiperazine | HCID 53167 | — |
| Product | Olanzapine | HCID 135398745 | — |
Reaction Steps
4-Amino-2-methyl-10H-thieno[2,3-b][1,5]benzodiazepine, hydrochloride (100 g) was refluxed in a mixture of N-methylpiperazine (349 mL), dimethylsulphoxide (465 mL) and toluene (465 mL) under a nitrogen atmosphere for 20 hours. The mixture was cooled to 50° C., and water (465 mL) was added at 50-55° C. in 20 min. Then the reaction mass was cooled to 5° C. and stirred for 2 h. The product was filtered and washed with water (100 mL, 20° C.). Dried the product at 60-70° C. under reduced pressure to give crude 2-Methyl-4-(4-methyl-1-piperazinyl)-10H-thieno[2,3-b][1,5]benzodiazepine or Olanzapine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106188B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-9a22724eeaae4377a527b7de9cebd067 |
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| Source note | uspto-grants-2012_01 |
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