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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620176Generated: October 29, 2026

Isopropyl iodide → HCID 14424032, compound

https://huagongshe.com/reaction/620176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 14424031HCID 14424031—
Solvent2-MethoxyethanolHCID 8019—
ProductHCID 14424032HCID 1442403254.7%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04820703
Source datasetuspto-grants-1989_04
ORD IDord-846f54c61bda4fa49581cbedace52387
Source noteuspto-grants-1989_04