HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953464Generated: October 25, 2026
4-Methylmorpholine → HCID 23298253, compound
https://huagongshe.com/reaction/1953464
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Cyclobutylmethanamine hydrochloride | HCID 21707944 | — |
| Reactant | 4-Chlorosulfonyl-3-(N,N-di-t-butoxycarbonylamino)-1-ethyloxycarbonylmethyl-2-pyridinone | HCID 23298250 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23298253 | HCID 23298253 | — |
Reaction Steps
NMM (1.43 mL, 13.0 mmol) was added to a stirred mixture of 4-chlorosulfonyl-3-(N,N-di-t-butoxycarbonylamino)-1-ethyloxycarbonylmethyl-2-pyridinone (as a mixture from Step H, 0.84 g) and cyclobutylmethylamine hydrochloride (348 mg, 2.86 mmol) in methylene chloride (15 mL). After 16 h the reaction was diluted with methylene chloride and washed with 10% citric acid solution. The organic layer was dried (Na2SO4) and evaporated. The residue was purified by flash column chromatography on silica (40% ethyl acetate/hexanes). HCl gas was bubbled through a stirred solution of the resulting compound in ethyl acetate (10 mL) at 0° C. for 15 min. The reaction was warmed to rt and after a further 3 h it was evaporated to give the title compound as a solid;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06117888 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-c9880aa6f3674fa69b86f03a7c17fc6d |
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| Source note | uspto-grants-2000_09 |
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