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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773881Generated: November 3, 2026

Sodium Hydroxide → Ammonium Hydroxide

https://huagongshe.com/reaction/1773881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantTrifluoromethanesulfonic acidHCID 62406—
Reactant4-Piperidinol, 1-methyl-HCID 66048—
ReactantHCID 86703962HCID 86703962—
SolventWaterHCID 962—
ProductAmmonium HydroxideHCID 14923—
ProductHCID 72694673HCID 72694673—

Reaction Steps

To 1-[2-(2-chlorophenyl)ethyl]-4-iodoimidazole-2-carbaldehyde (example 78B) (200 mg, 0.55 mmole) is added trifluoromethanesulfonic acid (2 mL). The purple solution is stirred at room temperature overnight, 4-hydroxy-N-methylpiperidine (190 mg, 1.65 mmole) is added and solution is stirred at room temperature for 2 hours. Water is added and the solution is made alkaline by adding 5N NaOH to pH 10. The aqueous phase is extracted with AcOEt. The organic phase is washed with water, brine, dried over MgSO4, filtered and the solvent removed under reduced pressure. The residue is purified by silica gel chromatography eluting with (CH2Cl2:MeOH) (100:0) to (90:10) then (CH2Cl2:MeOH:NH4OH) (9:1:0.1) to give 8-chloro-2-iodo-4-(1-methyl piperidin-4-yloxy)-9,10-dihydro-4H-3,10a-diaza-benzo[f]azulene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255101B2
Source datasetuspto-grants-2016_02
ORD IDord-ccaf0255d34b4c6e82de14840d502f06
Source noteuspto-grants-2016_02