Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86664045 | HCID 86664045 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86664046 | HCID 86664046 | — |
Reaction Steps
Ethyl 4-ethyl-1-[5-[2-(3-ethyl-5-methyl-2-oxo-1,3,5-triazinan-1-yl)-7-formyl-1,3-benzothiazol-5-yl]pyrimidin-2-yl]piperidine-4-carboxylate (33 mg, 0.058 mmol) was suspended in MeOH (2 mL) and treated with conc. H2SO4 (˜5 μL). The reaction was heated to 50° C. for 1.5 h then diluted with DCM and sat.NaHCO3(aq). The organic layer was separated and the aqueous layer extracted further with DCM (2×) before the combined DCM extracts were dried and the solvent evaporated to yield the crude product (35 mg). Crude product was used in the next step without further purification. MS: 557.16 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181234B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-e46f2fc98d7244febf26b99840aa8ff0 |
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| Source note | uspto-grants-2015_11 |
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