Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | L-Pyroglutamic Acid | HCID 7405 | — |
| Reactant | 4-Chlorophenylboronic acid | HCID 74299 | — |
| Product | HCID 42260685 | HCID 42260685 | — |
Reaction Steps
To a stirred suspension of (S)-5-oxo-pyrrolidine-2-carboxylic acid (775 mg, 6 mmol) in acetonitrile (10 mL) 1,8-diazabicyclo[5,4,0]undec-7-ene (DBU) (1.8 mL, 12 mmol) is added at room temperature. After 10 min di-μ-hydroxy-bis[N,N,N′,N′-tetramethylenediamine)-copper (II) chloride (Cu-TMEDA) (300 mg, 0.65 mmol) is added to the clear solution. The bluish green colored mixture is stirred for 10 min and 4-chlorophenylboronic acid (1 g, 6.4 mmol) is added. After 20 h acetonitrile is evaporated in vacuo, the concentrate taken up in ammonium chloride (150 mL) and the aqueous layer is washed with ethyl acetate (3×100 mL). The aqueous layer is cooled in an ice-bath, treated with 1 N sulfuric acid to pH 2 and extracted with ethyl acetate (3×100 mL). Combined organic extracts washed with brine (2×50 mL), dried over anhydrous Na2SO4 and solvent removed in vacuo to give the title compound as an off-white solid. ESI m/z 240 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629157B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-b2f55eb41a6e4e27b01e6083c3cfc169 |
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| Source note | uspto-grants-2014_01 |
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