HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127931Generated: November 1, 2026
Potassium Iodide → HCID 15571592, compound
https://huagongshe.com/reaction/127931
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-{4-[(3-Chloropropyl)sulfanyl]phenyl}acetamide | HCID 14005891 | — |
| Reactant | HCID 15571588 | HCID 15571588 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15571592 | HCID 15571592 | — |
Reaction Steps
A mixture of 3.6 g of 2,4-diamino-5-(3'-hydroxy-4'-methoxybenzyl)pyrimidine hydrochloride, 3.4 g of 3-(p-acetamidophenylthio)propyl chloride, 3.8 ml of methanol, 12 ml of an aqueous solution containing 0.027 mole of potassium hydroxide and 0.2 g of potassium iodide is heated at reflux for 20 hr. The mixture is cooled and filtered to remove a small amount of inorganic material. Water, (75 ml) is added to the filtrate, and the methanol is removed by vacuum distillation. After the addition of 50 ml of methylene chloride the mixture is stirred for 30 min. and then filtered to obtain a crystalline product. After twice recrystallizing from 50% aqueous ethanol the product 2,4-diamino-5-{3'-[3"-(p-acetamidophenylthio)propoxy]-4'-methoxybenzyl}pyrimidine, weighes 1.94 g and has m.p. 175°-177°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04258045 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-11226529870a4c3da0f0599f67bedf74 |
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| Source note | uspto-grants-1981_03 |
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