Isobutyl chloroformate → Boc-Ile-Pro-OBzl

HRID 1199231노트

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HRID 1199231 반응식
[NH:1]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[C@H:2]([C:7]([OH:9])=O)[C@H:3]([CH2:5][CH3:6])[CH3:4].C(OC(Cl)=O)C(C)C.C1C=CC2N(O)N=NC=2C=1.Cl.[NH:36]1[CH2:50][CH2:49][CH2:48][C@H:37]1[C:38]([O:40][CH2:41][C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1)=[O:39].C([O-])(O)=O.[Na+]>CN(C=O)C.CN1CCOCC1>[NH:1]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[C@H:2]([C:7]([N:36]1[CH2:50][CH2:49][CH2:48][C@H:37]1[C:38]([O:40][CH2:41][C:42]1[CH:43]=[CH:44][CH:45]=[CH:46][CH:47]=1)=[O:39])=[O:9])[C@H:3]([CH2:5][CH3:6])[CH3:4]

참가 물질

8

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온도
-15 °C

실험 절차

Boc-Ile-OH (12.01 g, 0.05 mole) in DMF (50 ml) was cooled to 0° C. and NMM (5.49 ml) was added. After cooling the solution to -15° C. isobutylchloroformate (6.48 ml) was added slowly while maintaining the temperature at -15° C. and stirred for 10 minutes at which time HOBt (7.65 g) was added and stirring was continued for additional 10 minutes. A pre-cooled solution of HCl-H-Pro-OBzl (12.09 g, 0.05 mole) in DMF (50 ml) and NMM (5.49 ml) was added to the above solution and the completeness of the reaction was followed by TLC. The reaction mixture was poured into a cold saturated NaHCO3 solution and stirred for one hour. The peptide was extracted into CHCl3 and washed with acid and base (0.5 N NaOH to remove HOBt), and on evaporating the solvent the product was obtained as an 92% yield. Rf1, 0.65. Anal. Calcd. for C 23 H34N2 ; O5 : C 66.00, H 9.19, N 6.69%. Found: C 65.58, H 8.28, N 7.13%.

후처리

  1. additionwas added slowly
  2. additionwas added
  3. stirringstirred for one hour
  4. extractionThe peptide was extracted into CHCl3
  5. washwashed with acid and base (0.5 N NaOH to remove HOBt)
  6. customon evaporating the solvent the product
  7. customwas obtained as an 92% yield

출처 및 근거

ORD 기록
ord-f980724288c94ce2838dc195d5816260
출처 데이터셋
uspto-grants-1990_02
특허 번호
US04898926

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