Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | N-cyano-N'-(5-chlorouracil-6-ylmethyl)-S-methylisothiourea | HCID 21699306 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178484943 | HCID 178484943 | 9% |
Reaction Steps
Next, 150 mg of the N-cyano-N′-(5-chlorouracil-6-ylmethyl)-S-methylisothiourea were suspended in ethanol (3 ml), followed by the addition of 2 ml of a 30% solution of methylamine in ethanol. The resulting mixture was heated at 50° C. for 3.5 hours under stirring. After an insoluble matter was filtered off, the filtrate was allowed to cool back to room temperature. A precipitate from the filtrate was collected by filtration, whereby 12 mg of the title compound were obtained (yield: 9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06255314B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-f49520e626de4475894c235815f6dcdb |
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| Source note | uspto-grants-2001_07 |
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