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Acetic Acid → N6-(1-Oxohexadecyl)-L-lysine

HRID 1704288
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HRID 1704288 반응식
[NH2:1][C@H:2]([C:8]([OH:10])=[O:9])[CH2:3][CH2:4][CH2:5][CH2:6][NH2:7].C(N(CC)CC)C.[C:18](ON1C(=O)CCC1=O)(=[O:34])[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33].C(O)(=O)C>O>[C:18]([NH:7][CH2:6][CH2:5][CH2:4][CH2:3][C@@H:2]([C:8]([OH:10])=[O:9])[NH2:1])(=[O:34])[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 5962L-LysineHCID 8471TriethylamineHCID 4620598Palmitic acid N-hydroxysuccinimide

생성물 1

HCID 100425N6-(1-Oxohexadecyl)-L-lysine수율 86%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To the solution of L-lysine (1 mmol) in water (2 ml) and triethylamine (0.27 ml, 2 mmol) 1 mmol of succinimidyl palmitate (suspended in 2 ml of acetone) was added at room temperature under stirring. Stirring of the reaction mixture was continued for 4h. Triethylamine was removed under reduced pressure, the precipitate was collected by filtration, washed with water and ethanol, crystallized from glacial acetic acid giving an 86% yield of the title compound. Analysis data are given in Table 2.

후처리

  1. stirringStirring of the reaction mixture
  2. customTriethylamine was removed under reduced pressure
  3. filtrationthe precipitate was collected by filtration
  4. washwashed with water and ethanol

출처 및 근거

ORD 기록
ord-e5237ac844f14b98bc5496c6a6836a6c
출처 데이터셋
uspto-grants-1978_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04126628

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