Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 59519054 | HCID 59519054 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59519081 | HCID 59519081 | 56% |
Reaction Steps
4-[3-Carboxymethyl-2-(4-fluoro-3-methoxyphenyl)-4-oxo-3,4-dihydroquinazolin-6-yl]-2,6,6-trimethylperhydro-1,4-diazepine-1-carboxylic acid tert-butyl ester (200 mg, 0.352 mmol), isopropylamine (208 mg, 299 uL, 3.52 mmol), 1-propanephosphonic acid cyclic anhydride (336 mg, 320 uL, 0.528 mmol) and DIPEA (135 mg, 186 uL, 1.06 mmol) were stirred at room temperature in DCM (15 mL) for 2 h. NaHCO3 (aq.) (15 mL) was added, the organic layer separated, dried (Na2SO4) and evaporated under reduced pressure. Crude product was purified by chromatography on silica gel with a gradient of DCM to DCM:MeOH (4:1, v/v) as eluent to afford 4-[2-(4-fluoro-3-methoxyphenyl)-3-(isopropylcarbamoylmethyl)-4-oxo-3,4-dihydroquinazolin-6-yl]-2,6,6-trimethylperhydro-1,4-diazepine-1-carboxylic acid tert-butyl ester (120 mg, 0.197 mmol, 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820649B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-a022b0617b28440785ea8193bcac4eb2 |
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| Source note | uspto-grants-2010_10 |
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