Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Olanzamine | HCID 135446208 | — |
| Solvent | Water | HCID 962 | — |
| Product | Olanzapine | HCID 135398745 | 86.5% |
Reaction Steps
4-Amino-2-methyl-10H-thieno-[2,3-b][1,5]benzodiazepine (100 g, 0.38 mol), N-methylpiperazine (250 mL, 2.5 vol) and 2-propanol (200 mL, 2 vol) were charged into a three-necked round bottom flask equipped with reflux condenser, overhead stirrer, and thermometer. The reaction mixture was heated to reflux at 102° C. under a nitrogen atmosphere overnight. The reaction mixture was allowed to cool to below 55° C. whereupon water (250 mL, 2.5 volumes) was added to precipitate out the solid. The light yellow solid was isolated by Buchner filtration and twice washed with 25% aqueous 2-propanol (100 mL) and then once with 2-propanol (100 mL). It was dried in vacuo to provide olanzapine in 86.5% yield (101.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863442B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-7d84afc7ef274298b5826691e9176ff0 |
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| Source note | uspto-grants-2011_01 |
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