HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298839Generated: October 29, 2026
4-Methylmorpholine → HCID 12050656, compound
https://huagongshe.com/reaction/2298839
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | (2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxylic acid | HCID 12050655 | — |
| Reactant | Benzyl N-(2-aminoethyl)carbamate hydrochloride | HCID 12715871 | — |
| Reactant | HCID 178526939 | HCID 178526939 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12050656 | HCID 12050656 | 90.9% |
Reaction Steps
N-methylmorpholine (0.47 ml) was added to a solution of (2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxylic acid (352.6 mg) [see Preparation 3], hydroxybenzotriazole hydrate (338.4 mg), N-benzyloxycarbonyl-1,2-diaminoethane hydrochloride (499.5 mg) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (552.7 mg) in dichloromethane (15 ml). The reaction mixture was stirred at room temperature for 18 hours, after which time the mixture was diluted with water and the organic layer was separated, dried over magnesium sulphate and the solvent removed under reduced pressure. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 1:1, changing to 1:9, by volume, hexane ethyl acetate to afford benzyl N-[2-([(2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinyl]carbonylamino)ethyl]carbamate (550 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06495549B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-57c01d94fca04e60a512a2e153e620af |
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| Source note | uspto-grants-2002_12 |
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