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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2,6-Lutidine → L-Lysine

HRID 1838795
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HRID 1838795 반응식
Br.[NH2:2][C@H:3]([C:9]([OH:11])=[O:10])[CH2:4][CH2:5][CH2:6][CH2:7][NH2:8].N1C(C)=CC=CC=1C.ClCC(OC(=O)CCl)=O>CN(C)C=O>[NH2:2][C@H:3]([C:9]([OH:11])=[O:10])[CH2:4][CH2:5][CH2:6][CH2:7][NH2:8]
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참가 물질

5

반응물 3

HCID 79372,6-LutidineHCID 10946Chloroacetic anhydrideHCID 56843351L-Lysine hydrobromide

생성물 1

HCID 5962L-Lysine

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

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온도
0 °C

실험 절차

250 mg (1.19 mmol) of poly-D/L-lysine hydrobromide (SIGMA; M: 30,000-70,000) are suspended in 4 ml of dimethylformamide under argon. The suspension is cooled down to 0° C. and 1.25 ml of 2,6-lutidine are added. A solution of 500 mg (2.93 mmol) of chloroacetic anhydride in 2 ml of dimethylformamide is added dropwise over the space of 15 min. The mixture is subsequently heated slowly to room temperature and stirred for 16 h. The working-up and purification take place in analogy with N(6)-chloroacetyl-poly-L-lysine. 210 mg (85%) of N(6)-chloroacetyl-poly-D/L-lysine B3 are obtained.

후처리

  1. temperatureThe mixture is subsequently heated slowly to room temperature
  2. custompurification

출처 및 근거

ORD 기록
ord-1809b6b3672a432283cf0d86c0d65563
출처 데이터셋
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06677164B1

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