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Diisopropylethylamine → HCID 59314384, compound

HRID 1047864
Notes
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Reaction equation

HRID 1047864 reaction equation
[CH2:1]([O:3][C:4]([C:6]1([NH2:15])[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7]1)=[O:5])[CH3:2].[F:16][CH:17]([F:29])[O:18][C:19]1[CH:27]=[CH:26][C:22]([C:23](O)=[O:24])=[C:21]([CH3:28])[CH:20]=1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C>>[CH2:1]([O:3][C:4]([C:6]1([NH:15][C:23](=[O:24])[C:22]2[CH:26]=[CH:27][C:19]([O:18][CH:17]([F:16])[F:29])=[CH:20][C:21]=2[CH3:28])[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7]1)=[O:5])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 10921653Ethyl 2-amino-2,3-dihydro-1H-indene-2-carboxylateHCID 59314174HCID 59314174, compound

Product 1

HCID 59314384HCID 59314384, compoundYield 89%

Procedure

2-Amino-indane-2-carboxylic acid ethyl ester (2) (250 mg, 1.2 mmol), 4-difluoromethoxy-2-methyl-benzoic acid (242) (246 mg, 1.2 mmol) and HATU (555 mg, 1.46 mmol) are taken in a vial, evacuated and refilled with nitrogen Anhydrous DMF (2 mL) is added and stirring is initiated. After few min, DIPEA (0.302 mL, 1.82 mmol) is added and stirred at RT overnight. Analysis by tlc of the reaction mixture (silica, 50% EtOAc/heptanes) indicates complete consumption of the starting amine. Water (10 mL) is added, extracted with EtOAc (3×5 mL), dried over Na2SO4, concentrated and the crude product is chromatographed on a 25 g silica gel column using 20-50% EtOAc in heptane as a gradient to afford 2-(4-difluoromethoxy-2-methyl-benzoylamino)-indan-2-carboxylic acid ethyl ester (415 mg, 89%).

Workup

  1. customevacuated
  2. additionrefilled with nitrogen Anhydrous DMF (2 mL)
  3. additionis added
  4. stirringstirred at RT overnight
  5. customconsumption of the starting amine
  6. additionWater (10 mL) is added
  7. extractionextracted with EtOAc (3×5 mL)
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated
  10. customthe crude product is chromatographed on a 25 g silica gel column

Sources & evidence

ORD record
ord-50f89c4933964ae4b02a56021b868ddd
Source dataset
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08569535B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes