5-Tert-butylthiophene-2-carboxylic acid → tert-butyl (5-(tert-butyl)thiophene-2-carbonyl)-L-tyrosinate

HRID 1775831노트

반응식

HRID 1775831 반응식
[C:1]([C:5]1[S:9][C:8]([C:10]([OH:12])=O)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[NH2:37][C@@H:38]([CH2:46][C:47]1[CH:52]=[CH:51][C:50]([OH:53])=[CH:49][CH:48]=1)[C:39]([O:41][C:42]([CH3:45])([CH3:44])[CH3:43])=[O:40]>CN(C=O)C>[C:1]([C:5]1[S:9][C:8]([C:10]([NH:37][C@H:38]([C:39]([O:41][C:42]([CH3:45])([CH3:44])[CH3:43])=[O:40])[CH2:46][C:47]2[CH:52]=[CH:51][C:50]([OH:53])=[CH:49][CH:48]=2)=[O:12])=[CH:7][CH:6]=1)([CH3:2])([CH3:3])[CH3:4]

참가 물질

5

실험 절차

Prepared using General Procedure 7. Into a solution of 5-(tert-butyl)thiophene-2-carboxylic acid (1.93 g, 10.0 mmol) in DMF (20 mL) were added HATU (4.56 g, 12.0 mmol) and TEA (4.18 mL, 30.0 mmol). The mixture was stirred at room temperature for 30 min and (S)-tert-butyl 2-amino-3-(4-hydroxyphenyl)propanoate (2.37 g, 10.0 mmol) was added. After 1 h, the reaction mixture was poured into 400 mL of ice-water and the solid was filtered. The solid was dissolved in DCM and EA, dried over MgSO4, concentrated, and purified by chromatography (EA/hexanes) to provide 3.6 g (89%) of tert-butyl (5-(tert-butyl)thiophene-2-carbonyl)-L-tyrosinate. LCMS-ESI (m/z) calculated for C22H29NO4S: 403.2. found: 426.1 [M+Na]+, tR=9.07 min (Method 2).

후처리

  1. customPrepared
  2. waitAfter 1 h
  3. filtrationthe solid was filtered
  4. dissolutionThe solid was dissolved in DCM
  5. dry with materialEA, dried over MgSO4
  6. concentrationconcentrated
  7. custompurified by chromatography (EA/hexanes)

출처 및 근거

ORD 기록
ord-4383e591810a4a0db9aa407d477f2444
출처 데이터셋
uspto-grants-2016_02
특허 번호
US09260427B2

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