Glycolic Acid → HCID 57437439, compound

HRID 2240831Notes

Reaction equation

HRID 2240831 reaction equation
[C:1](O)(=[O:4])[CH2:2][OH:3].CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.CCN(C(C)C)C(C)C.[NH2:37][CH2:38][CH:39]([OH:64])[CH2:40][O:41][C:42]1[CH:47]=[CH:46][C:45]([CH2:48][CH2:49][C:50]([C:52]2[S:53][C:54]([CH3:63])=[C:55]3[CH2:60][C:59]([CH3:62])([CH3:61])[CH2:58][CH2:57][C:56]=23)=[O:51])=[CH:44][CH:43]=1>C(Cl)Cl>[OH:4][CH2:1][C:2]([NH:37][CH2:38][CH:39]([OH:64])[CH2:40][O:41][C:42]1[CH:43]=[CH:44][C:45]([CH2:48][CH2:49][C:50](=[O:51])[C:52]2[S:53][C:54]([CH3:63])=[C:55]3[CH2:60][C:59]([CH3:61])([CH3:62])[CH2:58][CH2:57][C:56]=23)=[CH:46][CH:47]=1)=[O:3]

Participants

6

Procedure

To a solution of glycolic acid (1.5 eq.) in DCM (10 mL), TBTU (1.3 eq.) and DIPEA (4.0 eq.) is added. The mixture is stirred at rt for 10 min before the appropriate 3-[4-(3-amino-2-hydroxy-propoxy)-phenyl]-1-(3,5,5-trimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-propan-1-one (0.5-1.0 mmol, 1. eq.) is added. Stirring is continued at rt for 1 h before another portion of glycolic acid (0.7 eq.) and TBTU (0.6 eq.) is added. The mixture is stirred for another hour, is diluted with DCM and washed with sat. aq. NaHCO3 solution. The wash solutions are extracted back with DCM. The combined organic extracts are dried over MgSO4, filtered and the solvent is evaporated. The crude product is purified by chromatography on prep. TLC plates using DCM containing 5% of methanol to give the desired 2-hydroxy-N-(2-hydroxy-3-{4-[3-oxo-3-(3,5,5-trimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-propyl]-phenoxy}-propyl)-acetamide as an almost colourless foam.

Workup

  1. additionis added
  2. additionis added
  3. stirringThe mixture is stirred for another hour
  4. washwashed with sat. aq. NaHCO3 solution
  5. extractionThe wash solutions are extracted back with DCM
  6. dry with materialThe combined organic extracts are dried over MgSO4
  7. filtrationfiltered
  8. customthe solvent is evaporated
  9. customThe crude product is purified by chromatography on prep

Sources & evidence

ORD record
ord-b16badeb97444176a1380d39ec3f3674
Source dataset
uspto-grants-2010_05
Patent number
US07723378B2

Reaction notes

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