HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326496Generated: October 25, 2026
Piperazine → 2-Piperazin-1-yl-1,3-benzothiazole
https://huagongshe.com/reaction/326496
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2-Chlorobenzothiazole | HCID 11987 | — |
| Product | 2-Piperazin-1-yl-1,3-benzothiazole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05268477 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-a47fa78cb91a4e409cc0fd8cd9b14303 |
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| Source note | uspto-grants-1993_12 |
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