Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720779Generated: November 1, 2026

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

https://huagongshe.com/reaction/1720779

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. 1% 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 numberUS05506354
Source datasetuspto-grants-1996_04
ORD IDord-93780d1f062942aaa597f48a0306e775
Source noteuspto-grants-1996_04