HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → N-{4-[(Pyrimidin-2-yl)amino]benzoyl}-L-glutamic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-[4-(Pyrimidin-2-ylamino)-benzoylamino]-pentanedioic acid diethyl ester | HCID 67334207 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-{4-[(Pyrimidin-2-yl)amino]benzoyl}-L-glutamic acid | HCID 57728787 | 56.2% |
Reaction Steps
A solution of 2-[4-(pyrimidin-2-ylamino)-benzoylamino]-pentanedioic acid diethyl ester (250 mg, 0.62 mmol) in THF (4 mL) was added to MeOH (4 mL), followed by the addition of 1N NaOH solution (5 mL, 5 mmol, 8 equiv.). The mixture was stirred at room temperature overnight. Reaction was complete as determined by HPLC. Solvents were removed by rotavap and a small amount of water (5 mL) was added to make a homogeneous solution. 1N HCl was added dropwise until the solution reached a pH of 4. The solid precipitate was collected by filtration, washed with EtOAc, and dried in vacuum oven. The product N-[4-(pyrimidin-2-ylamino)benzoyl]-L-glutamic acid (120 mg) was isolated in 45% yield. MS (ESI) m/z 343.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07998965B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-ea0b7c8f664d4355b87b4b7b7c73ea63 |
| Source note | uspto-grants-2011_08 |