HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515644Generated: October 29, 2026
Dimethylformamide dimethyl acetal → HCID 178484363, compound
https://huagongshe.com/reaction/515644
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | (2S,5R)-tert-butyl 5-(N-(benzyloxy)-2-nitrophenylsulfonamido)-2-carbamothioylpiperidine-1-carboxylate | HCID 86701414 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178484363 | HCID 178484363 | 72% |
Reaction Steps
A mixture of (2S,5R)-tert-butyl 5-(N-(benzyloxy)-2-nitrophenylsulfonamido)-2-carbamothioylpiperidine-1-carboxylate (1.65 g, 3 mmol) and 1,1-dimethoxy-N,N-dimethylmethanamine (1.08 g, 9.0 mmol) in dry dioxane (20 mL) was stirred at 45° C. overnight. The reaction mixture was concentrated under vacuum and the residue was purified by silica gel column chromatography (1:1 petroleum ether/EtOAc) to give (2S,5R)-tert-butyl 5-(N-(benzyloxy)-2-nitrophenylsulfonamido)-2-((E)-(dimethylamino)methylenecarbamothioyl)piperidine-1-carboxylate (1.3 g, 72%) as a yellow solid. ESI-MS (EI+, m/z): 606 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108966B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-e6fe7fad13674f13a8a2644901eec901 |
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| Source note | uspto-grants-2015_08 |
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