Trifluoroacetic acid → [2-(1-Azido-2-{3-[2-(2,2,2-trifluoroacetylamino)-ethylcarbamoyl]phenoxy}ethoxy)ethoxy]acetic acid ethyl ester

HRID 1714091Notes

Reaction equation

HRID 1714091 reaction equation
[N:1]([CH:4]([O:16][CH2:17][CH2:18][O:19][CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22])[CH2:5][O:6][C:7]1[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=1C(O)=O)=[N+:2]=[N-:3].C1C(=O)N(OC(ON2C(=O)CCC2=O)=O)C(=O)C1.[F:44][C:45]([F:50])([F:49])[C:46](O)=[O:47].[NH2:51][CH2:52][CH2:53][NH:54][C:55](=[O:60])C(F)(F)F.C(N(C(C)C)CC)(C)C>CN(C1C=CN=CC=1)C.CN(C=O)C>[CH2:24]([O:23][C:21](=[O:22])[CH2:20][O:19][CH2:18][CH2:17][O:16][CH:4]([N:1]=[N+:2]=[N-:3])[CH2:5][O:6][C:7]1[CH:8]=[CH:12][CH:13]=[C:14]([C:55](=[O:60])[NH:54][CH2:53][CH2:52][NH:51][C:46](=[O:47])[C:45]([F:50])([F:49])[F:44])[CH:15]=1)[CH3:25]

Participants

8

Reactant 5

HCID 6422Trifluoroacetic acidHCID 81531DiisopropylethylamineHCID 229755N-(2-aminoethyl)-2,2,2-trifluoroacetamideHCID 676246Di(succinimido) carbonateHCID 86628347(2-Azido-2-(2-ethoxycarbonylmethoxy-ethoxy)-ethoxy]-benzoic acid

Product 1

HCID 59771759[2-(1-Azido-2-{3-[2-(2,2,2-trifluoroacetylamino)-ethylcarbamoyl]phenoxy}ethoxy)ethoxy]acetic acid ethyl esterYield 86.6%

Reagents, catalysts & solvents 2

HCID 142844-(Dimethylamino)pyridineCatalystHCID 6228DimethylformamideSolvent

Procedure

3-[(2-Azido-2-(2-ethoxycarbonylmethoxy-ethoxy)-ethoxy]-benzoic acid (0.212 g, 0.6 mmol) was stirred with N,N′-disuccinimidyl carbonate (0.184 g, 0.72 mmol) and DMAP (0.088 g, 0.72 mmol) in dry DMF (1 ml) at room temperature. After 10 minutes, trifluoroacetic acid salt of N-(2-amino-ethyl)-2,2,2-trifluoro-acetamide (0.194 g, 0.72 mmol) was added followed by diisopropylethylamine (DIPEA) (0.251 ml, 1.44 mmol). The reaction mixture was then stirred at room temperature for 17 hours. All the solvents were evaporated under reduced pressure and the residues were partitioned between DCM (50 ml) and aqueous NaH2PO4 (1 N, 50 ml). The aqueous layer was further extracted with DCM (2×25 ml). All the DCM extracts were combined, dried over MgSO4 and evaporated under reduced pressure. The residue was purified by column chromatography (1×20 cm). The title compound, eluted with 1% methanol in DCM, was obtained as an oil (0.255 g, 86.6%). ES-MS, m/z 490.10 (M−1).

Workup

  1. customAll the solvents were evaporated under reduced pressure
  2. customthe residues were partitioned between DCM (50 ml) and aqueous NaH2PO4 (1 N, 50 ml)
  3. extractionThe aqueous layer was further extracted with DCM (2×25 ml)
  4. dry with materialdried over MgSO4
  5. customevaporated under reduced pressure
  6. customThe residue was purified by column chromatography (1×20 cm)
  7. washThe title compound, eluted with 1% methanol in DCM

Sources & evidence

ORD record
ord-165c036f62a848e282f4de93cb1f7a42
Source dataset
uspto-grants-2010_09
Patent number
US07795424B2

Reaction notes

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