Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | HCID 14839498 | HCID 14839498 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14839507 | HCID 14839507 | — |
Reaction Steps
Iodine, 6.34 g, is added in small portions to a mixture of 6 g of 6-[4-(2-pyrimidinyl)-1-piperazinyl]-2-hexanone (Example A) and 3.8 g of thiourea. The resulting paste is heated at 110° C. overnight. The mixture is taken up into boiling water, filtered, and basified with ammonium hydroxide. Dichloromethane is used to extract the products which are purified by silica gel chromatography to afford 2 g of recovered starting ketone, 0.8 g of 4-methyl-5-[3-[4-(2-pyrimidinyl)-1-piperazinyl]propyl]-2-thiazolamine (Example 1); mp 152°-156° C.; and 1.2 g of 4-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]-2-thiazolamine (Example 1a); mp 101°-104° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04935424 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-cfbea890444642b0a820911574a8cd48 |
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| Source note | uspto-grants-1990_06 |
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