HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243569Generated: October 30, 2026
Benzenesulfonic Acid → HCID 131725981, compound
https://huagongshe.com/reaction/1243569
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonic Acid | HCID 7371 | — |
| Reactant | 8-Chloro-5-methyl-1-[1-(2-pyridinyl)-4-piperidinyl]-5,6-dihydro-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine | HCID 11237434 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131725981 | HCID 131725981 | 90.7% |
Reaction Steps
To a suspension of 8-Chloro-5-methyl-1-(3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-yl)-5,6-dihydro-4H-2,3,5,10b-tetraaza-benzo[e]azulene (25.3 g, 64 mmol) in methanol (250 ml) was added benzenesulfonic acid (20.3 g, 128 mmol). The yellow solution was heated to 60° C. for 1 hour and then allowed to cool to ambient temperature and stirred for 16 hours. The mixture was cooled in iced water for 1 hour before filtering under vacuum to afford a white granular solid which, after being dried at 50° C. under vacuum for 16 hours, afforded the title compound (41.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119088B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-1dc4e91889844637a00b47421c2ce0e1 |
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| Source note | uspto-grants-2006_10 |
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