Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | HCID 11658676 | HCID 11658676 | — |
| Solvent | Water | HCID 962 | — |
| Product | Temozolomide | HCID 5394 | 86.8% |
Reaction Steps
A 500 ml reaction vessel equipped with a magnetic stirrer and a reflux condenser was charged with Temozolomide hydrochloride (11.7 grams, 0.0507 mol), acetonitrile (79 ml), acetic acid (2.5 ml) and water (96.5 ml). The reaction mixture was heated to 60-63° C. and stirring was maintained at this temperature for about 10 minutes. The reaction mixture was filtered at this temperature and then cooled to 5° C. for about half an hour to enable crystallization. The crystals thus obtained were collected and washed with water (2×20 ml) and cold acetone (20 ml). The crystals were dried at 40° C. in vacuum to obtain 8.54 grams (0.044 mol) of free Temozolomide base (86.7% yield). Purity (by HPLC): 99.96%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612202B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-c0186e0b00f44217a3cc39fbeb4d5f8f |
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| Source note | uspto-grants-2009_11 |
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