Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 11510616 | HCID 11510616 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11618895 | HCID 11618895 | 87% |
Reaction Steps
To a solution of 1-(3-methanesulfonylamino-2,4-dioxo-7-trifluoromethyl-1,2,3,4-tetrahydro-quinazolin-6-yl)-1H-imidazole-4-carboxylic acid methyl ester (150 mg, 0.335 mmol) in 10 ml dimethylformamide are added 1.7 ml of 1 M aqueous sodium hydroxide solution and stirred at room temperature for one hour and at 50° C. for two hours. After cooling to room temperature the solvent is evaporated in vacuo, the residue taken up in water, acidified with 5 ml of 1 M hydrochloric acid and extracted three times with 15 ml each of dichloromethane. The organic layer is dried over sodium sulfate, filtered and evaporated to give 126 mg (0.29 mmol, 87%) of amorphous 1-(3-methanesulfonylamino-2,4-dioxo-7-trifluoromethyl-1,2,3,4-tetrahydro-quinazolin-6-yl)-1H-imidazole-4-carboxylic acid, ES-MS: m/z 434 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299085B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-3b3313673d114cc593e040601ea9378a |
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| Source note | uspto-grants-2012_10 |
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