تفاعل #92795

ord-3f81971b3c1a40db94d050ff4c49361c

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09447450B2uspto-grants-2016_09