Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 69227997 | HCID 69227997 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10254245 | HCID 10254245 | — |
| Product | HCID 21091661 | HCID 21091661 | 200.7% |
Reaction Steps
To a solution of 4-amino-2-(4-methyl-benzylamino)-butyric acid methyl ester HCl salt (923 mg, 3.13 mmol) and DIEA (1.08 mL, 6.26 mmol) in 100 mL of DCM was added carbonyldiimidazole (760 mg, 4.69 mmol). The reaction mixture was stirred for 1 hour, after which the solvents were evaporated. The residue was dissolved in 20 mL of MeOH:H2O (2:1) solution to which was added LiOH (150 mg, 6.26 mmol). The mixture was stirred at room temperature for 3 hours and then adjusted to pH ˜7 by adding Dowex-H+ resin. The solution was filtered, the solvent was evaporated, and the residue dried under vacuum to give the desired compound of Formula 304, 3-(4-methyl-benzyl)-2-oxo-hexahydro-pyrimidine-4-carboxylic acid (520 mg, 67%), which was taken on without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07211580B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-27d2749f39a1492cbcd0fde9f55b235d |
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| Source note | uspto-grants-2007_05 |
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