Triethylamine → (9-(3-Fluoro-5-(2-hydroxyethyl)benzyl)-1-oxa-4,9-diazaspiro[5.5]undecan-4-yl)(2-isopropylthiazol-5-yl)methanone

HRID 1689338Notes

Reaction equation

HRID 1689338 reaction equation
[O:1]1[C:6]2([CH2:11][CH2:10][N:9]([CH2:12][C:13]3[CH:14]=[C:15]([CH2:20][CH2:21][OH:22])[CH:16]=[C:17]([F:19])[CH:18]=3)[CH2:8][CH2:7]2)[CH2:5][NH:4][CH2:3][CH2:2]1.C(N(CC)CC)C.[CH:30]([C:33]1[S:34][C:35]([C:38](O)=[O:39])=[CH:36][N:37]=1)([CH3:32])[CH3:31].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F>CN(C=O)C>[F:19][C:17]1[CH:18]=[C:13]([CH:14]=[C:15]([CH2:20][CH2:21][OH:22])[CH:16]=1)[CH2:12][N:9]1[CH2:10][CH2:11][C:6]2([O:1][CH2:2][CH2:3][N:4]([C:38]([C:35]3[S:34][C:33]([CH:30]([CH3:32])[CH3:31])=[N:37][CH:36]=3)=[O:39])[CH2:5]2)[CH2:7][CH2:8]1

Participants

6

Reactant 4

HCID 8471TriethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 197863422-(Propan-2-yl)-1,3-thiazole-5-carboxylic acidHCID 579889902-(3-(1-Oxa-4,9-diazaspiro[5.5]undecan-9-ylmethyl)-5-fluorophenyl)ethanol

Product 1

HCID 57988964(9-(3-Fluoro-5-(2-hydroxyethyl)benzyl)-1-oxa-4,9-diazaspiro[5.5]undecan-4-yl)(2-isopropylthiazol-5-yl)methanone

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
0 °C

Procedure

A solution of 2-(3-(1-oxa-4,9-diazaspiro[5.5]undecan-9-ylmethyl)-5-fluorophenyl)ethanol (example 55, step c) (0.153 g) in DMF (7 mL) was treated with triethylamine (0.208 mL) followed by 2-isopropylthiazole-5-carboxylic acid (example 55, step b) (0.085 g). The mixture was cooled to 0° C. and HATU (0.245 g) was added. The reaction mixture was stirred for 2 hours at 20° C. The mixture was partitioned between ethyl acetate and brine, the organic layer was washed twice with brine, dried over sodium sulphate, filtered and the solvent evaporated under reduced pressure. The crude product was purified by flash silica chromatography using 2.5% methanol in dichloromethane with 1% triethylamine as solvent. Pure fractions were evaporated to dryness to afford the subtitled compound. Yield 0.130 g.

Workup

  1. customThe mixture was partitioned between ethyl acetate and brine
  2. washthe organic layer was washed twice with brine
  3. dry with materialdried over sodium sulphate
  4. filtrationfiltered
  5. customthe solvent evaporated under reduced pressure
  6. customThe crude product was purified by flash silica chromatography
  7. customPure fractions were evaporated to dryness

Sources & evidence

ORD record
ord-61e36bad85f446cd8701ce642cfe6d37
Source dataset
uspto-grants-2012_04
Patent number
US08148373B2

Reaction notes

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