HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285336Generated: November 1, 2026
4-Amino-1-methylpiperidine → HCID 9798459, compound
https://huagongshe.com/reaction/1285336
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Amino-1-methylpiperidine | HCID 2737531 | — |
| Reactant | HCID 23301798 | HCID 23301798 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 9798459 | HCID 9798459 | 68.7% |
Reaction Steps
A quantity of 3.5 gm (0.022 mol) of N,N'-carbonyldiimidazole is added to a suspension of 5 gm (0.02 mol) of 5,11-dihydro-6-oxo-6H-dibenz[b,e]azepin-11-carboxylic acid in 100 ml of tetrahydrofuran, and the mixture is heated to 40° C. for 30 minutes. Then, 2.5 gm (0.022 mol) of 4-amino-1-methylpiperidine are added, and the mixture is heated for a further two hours at 40° C. After cooling, the solvent is removed in vacuo, and the residue is purified by column chromatography on silica gel [ethylene chloride/methanol (9:1)]. Subsequently, 4.8 gm (68%) of the desired compound, M.p.: 230°-231° C., are obtained from the eluate. According to the mixed melting point, thin layer chromatography, and IR spectrum, the substance is identical to the product obtained in Example 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04567178 |
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| Source dataset | uspto-grants-1986_01 |
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| ORD ID | ord-13cb8797df504dba89138713dba6402d |
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| Source note | uspto-grants-1986_01 |
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