Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Reactant | HCID 118061221 | HCID 118061221 | — |
| Product | HCID 118061508 | HCID 118061508 | — |
Reaction Steps
tert-Butyl 3-(4-((tert-butoxycarbonyl)amino)-1-methyl-1H-pyrazol-3-yl)-2-oxoimidazolidine-1-carboxylate (7.61 g) was dissolved in 2M hydrogen chloride methanol solution (50 mL), and the mixture was stirred at 60° C. for 3 hr. The reaction mixture was ice-cooled, ethyl acetate (50 mL) was added thereto, and the precipitate was collected by filtration, and dried under reduced pressure to give the title compound (4.15 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321757B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-761606f9be1a4702b313cc698ded2094 |
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| Source note | uspto-grants-2016_04 |
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