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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682365Generated: November 2, 2026

Piperazine → 2-Piperazin-1-yl-1,3-benzothiazole

https://huagongshe.com/reaction/1682365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant2-ChlorobenzothiazoleHCID 11987—
Product2-Piperazin-1-yl-1,3-benzothiazoleHCID 592122—

Reaction Steps

2-Chlorobenzothiazole (5.00 g), is heated in alcohol (75 ml) with 3.05 g piperazine (3.05 g) for 20 hr. The mixture is partitioned between methylene chloride/ether and aqueous sodium bicarbonate, the phases are separated, the organic phase is dried with sodium sulfate and concentrated to give 2-piperazinobenzothiazole which is reacted at 70° in acetonitrile (200 ml) with 21-bromo-17α-hydroxypregna-4,9(11)-diene-3,20-dione (7.45 g) and potassium carbonate (2.44 g) for 6 hr and at 20°-25° for 3 days. The mixture is partitioned between methylene chloride and aqueous sodium bicarbonate, the phases are separated, the organic phase is dried with sodium sulfate and concentrated. The concentrate is chromatographed on silica gel eluting with methanol/methylene chloride (6/94) to give the title compound which is recrystallized from ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05175281
Source datasetuspto-grants-1992_12
ORD IDord-61b6f5f6c1104aaa89f720569f018630
Source noteuspto-grants-1992_12