HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672855Generated: October 31, 2026
Ethylamine tetrahydrofuran → HCID 67351604, compound
https://huagongshe.com/reaction/1672855
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylamine tetrahydrofuran | HCID 66726184 | — |
| Reactant | HCID 67351173 | HCID 67351173 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67351604 | HCID 67351604 | 94.9% |
Reaction Steps
(S)-5-[3-(7-Ethylamino-9-methanesulfonyl-6-oxo-2,3,3a,4-tetrahydro-1H,6H-5,8,10,10b-tetraazabenzo[e]azulen-5-yl)phenyl]-3-methyl-1,3,4-oxadiazol-2(3H)-one (23.6 mg, 0.0472 mmol) obtained in Step 1 was dissolved in THF (2.0 mL), and the mixture was stirred at 90° C. for 30 minutes under microwave (CEM; Discover; 250 watts) irradiation after adding a 2.0 mol/L ethylamine/THF solution (1.0 mL, 2.00 mmol). The mixture was further stirred at 90° C. for 30 minutes under microwave (CEM; Discover; 250 watts) irradiation after adding a 2.0 mol/L ethylamine/THF solution (0.049 mL, 0.0981 mmol). The mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound (Compound 158) (20.8 mg, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07998954B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-7e564497de2149d69fc1beed4addf608 |
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| Source note | uspto-grants-2011_08 |
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