HCID 131723025, compound → HCID 59977253, compound

HRID 1726763Notes

Reaction equation

HRID 1726763 reaction equation
[CH3:1][C:2]1[CH:24]=[C:23]([C:25]([NH:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[C:31]([OH:35])[CH:30]=2)=[O:26])[CH:22]=[C:21]([CH3:36])[C:3]=1[C:4]([NH:6][C@H:7]([C:17]([O:19][CH3:20])=[O:18])[CH2:8][NH:9]C(OC(C)(C)C)=O)=[O:5]>FC(F)(F)C(O)=O.ClCCl>[NH2:9][CH2:8][C@@H:7]([C:17]([O:19][CH3:20])=[O:18])[NH:6][C:4](=[O:5])[C:3]1[C:2]([CH3:1])=[CH:24][C:23]([C:25]([NH:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[C:31]([OH:35])[CH:30]=2)=[O:26])=[CH:22][C:21]=1[CH3:36]

Participants

4

Procedure

A solution of crude N-[2,6-dimethyl-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoyl]-3-[[(1,1-dimethylethoxy)carbonyl]amino]-L-alanine, methyl ester (144 mg, 0.235 mmol) in trifluoroacetic acid (2 mL) and dichloromethane (2 mL) was stirred at room temperature for 1 h. The reaction mixture was concentrated and ethyl acetate was added. The solution was washed with saturated aqueous sodium hydrogen carbonate, and the aqueous layer was back-extracted seven times with ethyl acetate. The combined organic layers were dried (MgSO4), filtered, and evaporated to give crude 3-amino-N-[2,6-dimethyl-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoyl]-L-alanine, methyl ester (104 mg, 110% of the theoretical amount).

Workup

  1. concentrationThe reaction mixture was concentrated
  2. additionethyl acetate was added
  3. washThe solution was washed with saturated aqueous sodium hydrogen carbonate
  4. extractionthe aqueous layer was back-extracted seven times with ethyl acetate
  5. dry with materialThe combined organic layers were dried (MgSO4)
  6. filtrationfiltered
  7. customevaporated

Sources & evidence

ORD record
ord-d981ea39565341a6acce8fb551814c9a
Source dataset
uspto-grants-2009_02
Patent number
US07491741B2

Reaction notes

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