HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131457Generated: October 25, 2026
(S)-2-(2-Methoxyethyl)piperazine → (S)-7-Chloro-10-[3-(2-methoxy-ethyl)-piperazin-1-yl]-2-methyl-4H-3-thia-4,9-diaza-benzo[f]azulene
https://huagongshe.com/reaction/131457
Participants
| Role | Name | HCID | Charge |
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| Reactant | (S)-2-(2-Methoxyethyl)piperazine | HCID 55287560 | — |
| Reactant | 7-chloro-2-methyl-4H-3-thia-4,9-diaza-benzo[f]azulen-10-ylamine hydrochloride | HCID 136388572 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylsulfoxide toluene | HCID 22340214 | — |
| Product | (S)-7-Chloro-10-[3-(2-methoxy-ethyl)-piperazin-1-yl]-2-methyl-4H-3-thia-4,9-diaza-benzo[f]azulene | HCID 136090361 | 60% |
Reaction Steps
Dissolve 7-chloro-2-methyl-4H-3-thia-4,9-diaza-benzo[f]azulen-10-ylamine hydrochloride (1.46 g, 4.86 mmol) and (S)-2-(2-methoxy-ethyl)-piperazine (2.1 g, 14.6 mmol) in dimethylsulfoxide/toluene (1:2)(18 ml), stir under nitrogen and heat in an oil bath at 130° C. for 28.5 hours. Stir 16 hours at ambient temperature. Dilute the mixture with water and ethyl acetate, and extract with ethyl acetate. Combine the ethyl acetate extracts, wash with water and brine, dry the organic phase (Na2SO4), filter and concentrate under reduced pressure. Chromatograph on silica gel (eluent: 0-10% 2N ammonia in methanol/dichloromethane) to give the title compound (1.14 g, 60%), Mass Spectrum (ESMS) 391/393 (M+1), mp 179-183° C. (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384934B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-0de79bc9bdcf4decb9130433baa099b5 |
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| Source note | uspto-grants-2008_06 |
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