HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350512Generated: October 31, 2026
Dimethyl Sulfoxide → 11-{(S)-3-[2-(3-Fluoro-phenyl)-ethyl]-piperazin-1-yl}-3-methyl-5H-dibenzo[b,e][1,4]diazepine
https://huagongshe.com/reaction/1350512
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-methyl-5H-dibenzo[b,e][1,4]diazepin-1-ylamine hydrochloride | HCID 21093525 | — |
| Reactant | (S)-2-(2-(3-Fluoro-phenyl)-ethyl)-piperazine | HCID 21093648 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 11-{(S)-3-[2-(3-Fluoro-phenyl)-ethyl]-piperazin-1-yl}-3-methyl-5H-dibenzo[b,e][1,4]diazepine | HCID 58860720 | 66.3% |
Reaction Steps
Combine 3-methyl-5H-dibenzo[b,e][1,4]diazepin-1-ylamine hydrochloride (400.0 mg, 1.54 mmol), (S)-2-[2-(3-Fluoro-phenyl)-ethyl]-piperazine (641.5 mg, 3.08 mmol), N,N-diisopropylethylamine (199.0 mg, 1.54 mmol), DMSO (0.7 ml), and toluene (2.8 ml). Stir and heat the mixture at 110° C. After 64 hours, cool the mixture to ambient temperature and then dilute it with ethyl acetate. Wash the organic layer with 0.1 N NaOH and brine. Dry (sodium sulfate) and concentrate the organic layer to residue. Purify the residue on silica gel using dichloromethane/methanol (90:10) to give 423.2 mg (66%) of a tan foam: mp 81°, dec; mass spectrum (ion spray): m/z 415.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07214673B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-f5bdfd117ce349e2bd6c4dc66c901cbc |
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| Source note | uspto-grants-2007_05 |
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