Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | HCID 21339348 | HCID 21339348 | — |
| Reactant | HCID 131723227 | HCID 131723227 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 9933767 | HCID 9933767 | 57% |
Reaction Steps
Cyanuric chloride (33 mg, 0.18 mmol) was added to a solution of N-[N-((4-dimethylaminophenyl)sulfonyl)-L-leucinyl]-L-homophenylalaninamide (80 mg, 0.18 mmol) in DMF (2 mL) at 0° C. After stirring for 2h, the reaction was quenched by addition of satd. NaHCO3, filtered, diluted with EtOAc, washed sequentially with H2O (×5), brine, dried over Na2SO4, and concentrated giving a yellow foam. The crude residue was fractionated by preparative HPLC (65% AcCN/H2O/0.1% TFA) giving the title compound (47 mg, 57%) as a white solid, m.p. 46-48° C. 1H NMR (400 MHz, CDCl3): δ: 7.74(2H, d, J=9), 7.37-7.34 (2H, m), 7.30-7.26 (2H, m), 7.23-7.21 (3H, m), 6.79 (1H, d, J=8.5), 4.91 (1H, bs), 4.70 (1H, ddd, J=8, 8, 8), 3.68-3.73 (1H, m), 3.06 (3H, s), 2.84-2.76 (2H, m), 2.16-2.09(2H, m), 1.63-1.56 (2H, m), 1.42-1.37 (1H, m), 0.88 (3H, d, J=6), 0.71 (3H, d, J=6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06395897B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-2ca5bf24b62a4060b3376badd5f4f7bc |
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| Source note | uspto-grants-2002_05 |
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