Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 20034502 | HCID 20034502 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13910039 | HCID 13910039 | — |
Reaction Steps
0.5 g of the sodium salt of ethyl mercaptan was added to 30 ml of anhydrous tetrahydrofuran. 1.7 g of 5-chloro-4-{2-[4-(2-chloroethyl)-2-methylphenoxy]ethylamino]-6-methylpyrimidine was added to the mixture, which was then heated for 3 hours whilst stirring. At the end of this time, water was added to the mixture, and the oily product which separated was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous sodium sulfate. The ethyl acetate was removed by distillation under reduced pressure. The oily product obtained was subjected to column chromatography (Wakogen C-200, eluted with a 2:1 by volume mixture of toluene and ethyl acetate), to afford 1.2 g of the title compound as a pale yellow oily liquid, n20.8 =1.5478.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04845097 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-138222848f5547ba87f711673f5ca1f5 |
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| Source note | uspto-grants-1989_07 |
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