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Trifluoroacetic acid → (2R)-2-(2-aminoethylamino)-3-phenylpropionic acid methyl ester

HRID 581193
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인쇄 미리보기

반응식

HRID 581193 반응식
[CH3:1][O:2][C:3](=[O:23])[C@H:4]([NH:12][CH2:13][CH2:14][NH:15]C(OC(C)(C)C)=O)[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.FC(F)(F)C(O)=O>C(Cl)Cl>[CH3:1][O:2][C:3](=[O:23])[C@H:4]([NH:12][CH2:13][CH2:14][NH2:15])[CH2:5][C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 54571530(2R)-2-(2-(tert-butoxycarbonylamino)ethylamino)-3-phenylpropionic acid methyl ester

생성물 1

HCID 54002275(2R)-2-(2-aminoethylamino)-3-phenylpropionic acid methyl ester수율 125.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

(2R)-2-(2-(tert-Butoxycarbonylamino)ethylamino)-3-phenylpropionic acid methyl ester (1.32 g; 4.094 mmol) was dissolved in methylene chloride (10 ml) and trifluoroacetic acid (10 ml) was added. The reaction mixture was stirred for 1 hour at room temperature. The solvent was evaporated in vacuo and the residue was dissolved in methylene chloride (5 ml) and evaporated in vacuo. Methylene chloride (5 ml) was added and evaporated in vacuo to afford 1.14 g of (2R)-2-(2-aminoethylamino)-3-phenylpropionic acid methyl ester as a trifluoroacetate salt.

후처리

  1. customThe solvent was evaporated in vacuo
  2. dissolutionthe residue was dissolved in methylene chloride (5 ml)
  3. customevaporated in vacuo
  4. additionMethylene chloride (5 ml) was added
  5. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-c18f76108796453d819671c1d1ec5c78
출처 데이터셋
uspto-grants-1999_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05919777

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