HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6914Generated: October 29, 2026
Benzylamine → 4-(4-Benzyl-5-methyl-4H-[1,2,4]triazol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/6914
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 1-Boc-4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidine | HCID 21098364 | — |
| Catalyst | Magnesium Chloride | HCID 5360315 | — |
| Product | 4-(4-Benzyl-5-methyl-4H-[1,2,4]triazol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester | HCID 23544071 | 70.4% |
Reaction Steps
4-(5-Methyl-[1,3,4]oxadiazol-2-yl)-piperidine-1-carboxylic acid tert-butyl ester (5 g, 18.7 mmol) (see reference WO 0039125), benzylamine (2.5 ml, 22 mmol) and magnesium chloride (100 mg) were heated at 150° C. for 1 hour, a further quantity of benzylamine (2.5 ml, 22 mmol) was added and the mixture was heated at 150° C. for 4 hours. The reaction mixture was cooled to room temperature and the reaction mixture was purified by chromatography on silica gel using methanol in dichloromethane as eluant (3:97). The material isolated was triturated with diethyl ether to give the title compound as a white solid (4.69 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07084145B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-f6db3128a3104baab6ac26020f6aaa80 |
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| Source note | uspto-grants-2006_08 |
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