HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237731Generated: November 1, 2026
HCID 59849018, compound → HCID 86613530, compound
https://huagongshe.com/reaction/2237731
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59849018 | HCID 59849018 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Methylamine | HCID 6329 | — |
| Product | HCID 86613530 | HCID 86613530 | — |
Reaction Steps
A solution of 0.050 g of tert-butyl {3(S)-[4-methoxy-3-(3-methoxypropoxy)benzyl]-4-methyl-1(S)-(R)-oxiranylpentyl}carbamate (Example 1b) in 1.0 ml of isopropanol and 0.10 ml of methylamine is stirred at 60° C. over 2 hours. The reaction mixture is concentrated by evaporation to dryness. The residue is dissolved in 2 ml of dichloromethane, admixed successively with 0.017 ml of pyridine and 0.026 ml of acetic anhydride and stirred at room temperature over 1 hour. The reaction solution is admixed with water and extracted with tert-butyl methyl ether (2×). The combined organic phases are washed successively with 1M HCl, water and brine, dried over sodium sulphate and concentrated by evaporation. The title compound is obtained from the residue by means of flash chromatography (SiO2 60F) as a slightly yellowish oil. Rf=0.13 (95:5 dichloromethane-methanol); Rt=4.47 (gradient I).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07718675B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-c6bcffeee5b842d3877d6288cfb76264 |
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| Source note | uspto-grants-2010_05 |
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