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Diisopropylethylamine → N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-3-methyl-1,2-benzisoxazole-6-carboxamide

HRID 2306663
Notes
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Reaction equation

HRID 2306663 reaction equation
[CH3:1][C:2]1[C:6]2[CH:7]=[CH:8][C:9]([C:11]([OH:13])=O)=[CH:10][C:5]=2[O:4][N:3]=1.[CH3:14][CH2:15]N(C(C)C)C(C)C.CN(C(ON1N=[N:38][C:33]2[CH:34]=[CH:35][CH:36]=[N:37][C:32]1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F>CN(C=O)C>[N:37]12[CH2:36][CH2:35][CH:34]([CH2:14][CH2:15]1)[C@@H:33]([NH:38][C:11]([C:9]1[CH:8]=[CH:7][C:6]3[C:2]([CH3:1])=[N:3][O:4][C:5]=3[CH:10]=1)=[O:13])[CH2:32]2
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 226100463-Methylbenzo[d]isoxazole-6-carboxylic acid

Product 1

HCID 12132426N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-3-methyl-1,2-benzisoxazole-6-carboxamideYield 73.2%

Reagents, catalysts & solvents 1

HCID 6228
Dimethylformamide
Solvent

Procedure

3-Methyl-1,2-benzisoxazole-6-carboxylic acid (139 mg, 0.78 mmole) is combined with (3R)-aminoquinuclidine dihydrochloride (156 mg, 0.78 mmole) and DIEA (272 μL, 1.56 mmole) in 3 ml DMF under nitrogen. The mixture is treated with HATU (296 mg, 0.78 mmole), and the reaction is stirred overnight at rt. The volatiles are removed in vacuo and the residue is partitioned between 1×10 ml 10% MeOH/CHCl3 and 1×10 ml 1:1 saturated sodium chloride/conc. NH4OH. The aqueous layer is washed with 1×10 ml CHCl3 and the combined organic layer is dried over K2CO3. The dried organic layer is concentrated in vacuo to give an amber residue. The crude material is chromatographed over 15 g silica gel (230-400 mesh) eluting with 7% MeOH/CHCl3+1% conc. NH4OH. The appropriate fractions are combined and concentrated to give a pale foam. The foam is crystallized from Et2O to provide 163 mg (72%) of N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-3-methyl-1,2-benzisoxazole-6-carboxamide as an off-white solid. MS (EI) m/z: 285 (M+).

Workup

  1. customThe volatiles are removed in vacuo
  2. customthe residue is partitioned between 1×10 ml 10% MeOH/CHCl3 and 1×10 ml 1:1 saturated sodium chloride/conc
  3. washThe aqueous layer is washed with 1×10 ml CHCl3
  4. dry with materialthe combined organic layer is dried over K2CO3
  5. concentrationThe dried organic layer is concentrated in vacuo
  6. customto give an amber residue
  7. customThe crude material is chromatographed over 15 g silica gel (230-400 mesh)
  8. washeluting with 7% MeOH/CHCl3+1% conc. NH4OH
  9. concentrationconcentrated
  10. customto give a pale foam
  11. customThe foam is crystallized from Et2O

Sources & evidence

ORD record
ord-9daff107ae114a189a4f957802f2ce88
Source dataset
uspto-grants-2004_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06828330B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes