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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074409Generated: October 25, 2026

Hydrochloric Acid → 5-(4-Methyl-4-oxidopiperazino)-imidazo[2,1-b][1,3,5]benzothiadiazepine hydrochloride

https://huagongshe.com/reaction/1074409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPentiapineHCID 54742—
Reactantm-Chloroperbenzoic acidHCID 70297—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product5-(4-Methyl-4-oxidopiperazino)-imidazo[2,1-b][1,3,5]benzothiadiazepine hydrochlorideHCID 15586419—

Reaction Conditions

Temperature0 °C

Reaction Steps

To the solution of 88 mg of 5-(4-methylpiperazino)-imidazo[2,1-b][1,3,5]benzothiadiazepine in 1 ml of methylene chloride, 74 mg of m-chloroperbenzoic acid are added at 0° C. The mixture is stirred at 0° C. overnight; this is diluted with 1 ml of ether, one equivalent of ethereal hydrochloric acid solution is added and the resulting precipitate is collected. Recrystallization from methanol-ethyl acetate yields 5-(4-methyl-4-oxidopiperazino)-imidazo[2,1-b][1,3,5]benzothiadiazepine hydrochloride, melting at 155° with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04391808
Source datasetuspto-grants-1983_07
ORD IDord-bd76b2b5f6484aedb9e1051a75695721
Source noteuspto-grants-1983_07