HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658840Generated: October 31, 2026
Ammonium Hydroxide → HCID 21525722, compound
https://huagongshe.com/reaction/1658840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 5-(Piperidin-1-yl)pentan-2-one--hydrogen chloride (1/1) | HCID 108987 | — |
| Reactant | HCID 12268147 | HCID 12268147 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 21525722 | HCID 21525722 | 39.7% |
Reaction Steps
A solution of 5-piperidino-2-pentanone hydrochloride (3.4g.) and 5-amino-10,11-dihydro-5H-dibenz[b,f]azepine hydrochloride (4.2g.) in isopropyl alcohol (50 ml.) was warmed on a steam bath in a nitrogen atmosphere for thirty minutes, cooled and treated with concentrated ammonium hydroxide. The resulting mixture was extracted with ether and the ether extract was washed with water and dried. The resulting solution in ether of the free base 2-(2-piperidinoethyl)-1-methyl-6,7-dihydroindolo[1,7-ab][1]benzazepine was treated with ethanolic hydrogen chloride. The precipitate was collected and a suspension thereof in acetone-isopropyl alcohol was heated, cooled, filtered and recrystallized from methyl alcohol to give 2-(2-piperidinoethyl)-1-methyl-6,7-dihydroindolo[1,7-ab][1]benzazepine hydrochloride (2.5g.), m.p. 291°-293°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03966762 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-0913819ece22428c9811ebdb35373547 |
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| Source note | uspto-grants-1976_06 |
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