Reaktion #92795

ord-3f81971b3c1a40db94d050ff4c49361c

Reaktionsgleichung

CC(C)C[C@H](NC(=O)OC(C)(C)C)C(=O)Nc1ccc2c(ccc3nc(C#N)sc32)c1
7-(Boc-leucinyl)aminonaphtho[2,1-d]thiazole-2-carbonitrile
CSc1ccccc1
thioanisole
Cl.N[C@H](CS)C(=O)O.O
D-cysteine hydrochloride hydrate
O=C([O-])[O-].[K+].[K+]
potassium carbonate
O=C(O)C(F)(F)F
Trifluoroacetic acid
CC(C)C[C@H](N)C(=O)Nc1ccc2c(ccc3nc(C4=NC(C(=O)O)CS4)sc32)c1
2-(7-(Leucinyl)aminonaphtho[2,1-d]thiazol-2-yl)-4,5-dihydrothiazole-4-carboxylic acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigesolvents were removed under reduced pressure
  2. 2
    Sonstigethe remaining residue triturated with ether
  3. 3
    workup.WAITAfter 20 min
  4. 4
    Filtrationthe reaction was filtered
  5. 5
    Sonstigethe product was isolated by preparative HPLC
  6. 6
    Wascheneluting with 2→50% MeCN in 0.1% formic acid

Vorschrift

7-(Boc-leucinyl)aminonaphtho[2,1-d]thiazole-2-carbonitrile (69 mg, 0.16 mmol) was combined with 0.5 mL of thioanisole and 1.5 mL of DCM and stirred in an ice bath. Trifluoroacetic acid (1.5 mL) was added, and the reaction monitored by HPLC. After 1 h, solvents were removed under reduced pressure, and the remaining residue triturated with ether. The resulting solid was taken up in MeCN/H2O and treated with D-cysteine hydrochloride hydrate (55 mg, 0.31 mmol) and potassium carbonate (55 mg, 0.40 mmol). After 20 min, the reaction was filtered and the product was isolated by preparative HPLC eluting with 2→50% MeCN in 0.1% formic acid. Calcd for C21H23N4O3S2 (M+H): 443.1. found 443.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09447450B2uspto-grants-2016_09