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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109925Generated: October 30, 2026

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

https://huagongshe.com/reaction/1109925

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 numberUS05322943
Source datasetuspto-grants-1994_06
ORD IDord-6870f11ca5eb489b85cd746d82026180
Source noteuspto-grants-1994_06