تفاعل #1596965

ord-0636f40ae1b846aa92185b81c9594483

معادلة التفاعل

CC(C)(C)OC(=O)[C@@H](N)CCC(=O)OCc1ccccc1.Cl
L-Glu(OBn)-OtBu hydrochloride
O=C(OC(Cl)(Cl)Cl)OC(Cl)(Cl)Cl
triphosgene
CC(C)(C)OC(=O)[C@@H](N)CCCCNC(=O)OCc1ccccc1
L-Lys(Z)-OtBu
CCN(CC)CC
triethylamine
CC(C)(C)OC(=O)[C@H](CCCCNC(=O)OCc1ccccc1)NC(=O)N[C@@H](CCC(=O)OCc1ccccc1)C(=O)OC(C)(C)C
(9S,13S)-15-benzyl 13,9-di-tert-butyl 3,11-dioxo-1-phenyl-2-oxa-4,10,12-triazapentadecane-9,13,15-tricarboxylate

المذيبات

ظروف التفاعل

درجة الحرارة
-78°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITto come to room temperature over a period of 1 h
  2. 2
    workup.STIRRINGstirred at room temperature overnight
  3. 3
    أخرىThe reaction was quenched with 1N HCl
  4. 4
    استخلاصextracted with DCM
  5. 5
    أخرىThe organic layer was dried
  6. 6
    تركيزconcentrated under reduced pressure
  7. 7
    أخرىthe residue was purified

الإجراء التجريبي

To a solution of L-Glu(OBn)-OtBu hydrochloride (3.13 mg, 9.49 mmol) and triphosgene (923 mg, 3.13 mmol) in DCE (70 mL) cooled to −78° C. was added triethylamine (2.80 mL) under nitrogen. After stirring at −78° C. for 2 h, a solution of L-Lys(Z)-OtBu (3.88 g, 10.40 mmol) and TEA (1.5 mL) in DCE (10 mL) was added. The mixture was allowed to come to room temperature over a period of 1 h and stirred at room temperature overnight. The reaction was quenched with 1N HCl, and extracted with DCM. The organic layer was dried and concentrated under reduced pressure and the residue was purified utilizing a Biotage SP4 to afford (9S,13S)-15-benzyl 13,9-di-tert-butyl 3,11-dioxo-1-phenyl-2-oxa-4,10,12-triazapentadecane-9,13,15-tricarboxylate as a colorless oil (4.71 g, 76%). 1H NMR (400 MHz, CDCl3) δ 7.34-7.29 (m, 10H), 5.13-5.04 (m, 6H), 4.97 (brs, 1H), 4.38-4.28 (m, 2H), 3.18-3.14 (m, 2H), 2.50-2.35 (m, 2H), 2.19-2.10 (m, 1H), 1.94-1.85 (m, 1H), 1.79-1.72 (m, 1H), 1.58-1.33 (m, 21H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08211402B2uspto-grants-2012_07