HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620176Generated: October 29, 2026
Isopropyl iodide → HCID 14424032, compound
https://huagongshe.com/reaction/620176
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 14424031 | HCID 14424031 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | HCID 14424032 | HCID 14424032 | 54.7% |
Reaction Steps
A mixture of 0.5 g of thienotriazolodiazepine compound obtained in Example 5, 0.2 g of potassium hydroxide and 0.62 g of isopropyl iodide in 20 ml of 2-methoxyethanol is stirred at 90° C. for 4 hours, and then the resulting mixture is concentrated to dryness. The residue is dissolved in 50 ml of chloroform, washed with water and dried over anhydrous magnesium sulfate. After separating by filtration, the filtrate is concentrated under reduced pressure and the residue is crystallized from isopropyl ether-ethyl acetate to give 0.3 g of 4-(2-chlorophenyl)-2-[2-(4-isopropoxyphenyl)ethyl]-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine as colorless crystals, melting at 121°-124° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04820703 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-846f54c61bda4fa49581cbedace52387 |
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| Source note | uspto-grants-1989_04 |
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