Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | HCID 21517736 | HCID 21517736 | — |
| Product | HCID 21517701 | HCID 21517701 | — |
Reaction Steps
23 gm (0.07 mol) of 6-ethoxy-2-methylthio-5-nitro-4-thiomorpholino-pyrimidine were added to 68 gm (0.8 mol) of molten piperazine, and the mixture was heated at 110°C for 1 hour. After cooling, ice water was added to the reaction mixture, and the yellow precipitate formed thereby was suction-filtered off, washed with water and recrystallized from isopropanol. Yield: 18 gm (70% of theory); m.p. 166.5°-168.5°C
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03975384 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-c33b74653a1248e0959d81be87c28313 |
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| Source note | uspto-grants-1976_08 |
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