HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484307Generated: October 28, 2026
Ammonium Chloride → HCID 19747289, compound
https://huagongshe.com/reaction/484307
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-chloro-N-methylpiperidine | HCID 79342 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 19747241 | HCID 19747241 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19747289 | HCID 19747289 | 47% |
Reaction Steps
Into a tetrahydrofuran (THF) solution of a Grignard reagent prepared from 6.7 g of N-methyl-4-chloropiperidine and 1.2 g of magnesium, 4.68 g of 8-cyano5,6-dihydro-1H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-one (the compound prepared in Referential Example 1) were added under ice cooling. After the resultant mixture was stirred for 3 hours at room temperature, a saturated aqueous solution of ammonium chloride was added, followed by stirring for 15 minutes. The reaction mixture was then extracted with chloroform. The Extract was dried over anhydrous Na2SO4 and then filtered. The filtrate so obtained was concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column and, from relevant fractions eluted with chloroform:methanol (50:1), 3.1 g of 8-cyano-6,11-dihydro-11-(1-methyl-4-piperidyl)-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ol were obtained (yield: 47%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05231101 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-5d637f8a96ff427689f211e33eaf18f2 |
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| Source note | uspto-grants-1993_07 |
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