HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451865Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 59201564, compound
https://huagongshe.com/reaction/451865
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 59201451 | HCID 59201451 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59201564 | HCID 59201564 | 45.8% |
Reaction Steps
A solution of DMSO (0.82 g, 10.47 mmol) in 10 mL of dry CH2Cl2, under protection of N2, was cooled to −78° C., followed by the slow, dropwise addition of oxalyl chloride (0.664 g, 5.23 mmol). After addition the mixture was stirred 2 hr at −65° C., then the solution of (S)-tert-butyl 1-(4-hydroxycyclohexyl)-3-(N-methyl-N-(benzyloxycarbonyl)amino)propan-2-ylcarbamate (1.1 g, 2.62 mmol) was added dropwise. After addition, the mixture was stirred 3 hr at −30° C. The reaction was quenched with Et3N (4 mL) and stirred 10 min, then saturated NaHCO3 (10 mL) was added. The aqueous layer was extracted 3 times with CH2Cl2 (3×20 mL). The CH2Cl2 layer was washed with 10% citric acid solution (20 mL), followed by saturated NaHCO3, brine, then dried over Na2SO4. After filtration, solvent removal gave crude product (1 g), which was purified by preparative TLC to give (S)-tert-butyl 1-(N-methyl-N-(benzyloxycarbonyl)amino)-3-(4-oxocyclohexyl)propan-2-ylcarbamate (500 mg, 1.2 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08487108B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-38ae103994514255ba8e825e7dc70508 |
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| Source note | uspto-grants-2013_07 |
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