Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 68705716 | HCID 68705716 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67487426 | HCID 67487426 | 95.2% |
Reaction Steps
tert-Butyl 4-(5-(3-(2-methylpyridin-3-yloxy)-5-(pyridin-2-ylthio)pyridin-2-ylamino)-1,2,4-thiadiazol-3-yl)azepane-1-carboxylate (70.4 mg, 0.119 mmol) was dissolved in CH2Cl2 (2 mL) and TFA (2 mL) was added. After 10 minutes the reaction was concentrated and placed on high vacuum pump to remove excess TFA. The residue was dissolved in CH2Cl2 (2 mL) and triethylamine (82.3 μL, 0.591 mmol) and acetic anhydride (16.7 μL, 0.177 mmol) were added. After 10 minutes the reaction was partitioned between saturated aqueous NaHCO3 and EtOAc, dried over sodium sulfate, filtered and concentrated. The residue was purified over silica gel (10% methanol in EtOAc) to afford 1-(4-(5-(3-(2-methylpyridin-3-yloxy)-5-(pyridin-2-ylthio)pyridin-2-ylamino)-1,2,4-thiadiazol-3-yl)azepan-1-yl)ethanone dihydrochloride (68.2 mg, 0.112 mmol, 95.2% yield) as a solid after HCl salt formation. Mass spectrum (apci) m/z=534.2 (M+H-2HCl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362037B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-436f1fb73ec248c4946a9d293b963142 |
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| Source note | uspto-grants-2013_01 |
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