반응 #1596965

ord-0636f40ae1b846aa92185b81c9594483

반응 방정식

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

용매

반응 조건

온도
-78°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08211402B2uspto-grants-2012_07