Diisopropylethylamine → HCID 58284927, compound

HRID 2279221Notes

Reaction equation

HRID 2279221 reaction equation
[CH2:1]([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[N+:20]([O-])=O)[CH:10]([CH2:23][C:24]([OH:26])=O)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)C2N=CC=CC=2N=N1.C(N(C(C)C)CC)(C)C>[Pt].CO.O>[CH2:1]([N:8]1[CH2:13][CH2:12][N:11]2[C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[NH:20][C:24](=[O:26])[CH2:23][CH:10]2[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

7

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 58284941HCID 58284941, compound

Product 1

HCID 58284927HCID 58284927, compound

Reagents, catalysts & solvents 3

HCID 23939PlatinumCatalystHCID 887MethanolSolventHCID 962WaterSolvent

Procedure

Platinum on carbon (5%, 30 mg) was added to a solution of the product of Example 26B (0.67 g, 1.88 mmol) in methanol (100 mL). The reaction flask was evacuated and purged with nitrogen (5 cycles) and then with hydrogen (5 cycles), and the suspension was stirred under hydrogen (1 atm) for 18 hours. The reaction flask was evacuated and purged with nitrogen (5 cycles), and the mixture was filtered through diatomaceous earth with ethyl acetate (50 mL) and methanol (50 mL) rinses. The filtrate was concentrated under vacuum and the residue was dissolved in N,N-dimethylformamide (8 mL). O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (720 mg, 1.89 mmol) and diisopropylethylamine (0.395 mL, 2.262 mmol) were added, and the solution was stirred at room temperature for 3 hours. The mixture was diluted with water (50 mL) and extracted with ethyl acetate (2×50 mL). The combined extracts were washed successively with 1 N NaOH (50 mL) and brine (40 mL), and then concentrated under vacuum. The residue was purified by flash chromatography (SiO2 eluted with CH2Cl2—CH3OH, 100:0-95:5) to provide the title compound: 1H NMR (300 MHz, CD3OD) δ ppm 1.98 (dd, J=13.4, 1.2 Hz, 1H), 2.27 (dt, J=11.4, 3.1 Hz, 1H), 2.40 (t, J=10.9 Hz, 1H), 2.67 (dd, J=13.2, 7.5 Hz, 1H), 2.82-2.89 (m, 1H), 2.89-2.97 (m, 1H), 3.01-3.09 (m, 1H), 3.22 (dd, J=11.5, 2.7 Hz, 1H), 3.35-3.44 (m, 1H), 3.61 (s, 2H), 6.98 (dd, J=8.1, 1.7 Hz, 1H), 7.03 (td, J=7.3, 1.7 Hz, 1H), 7.10-7.22 (m, 2H), 7.25-7.39 (m, 5H); MS (DCI) m/z 308 (M+H)+.

Workup

  1. customThe reaction flask was evacuated
  2. custompurged with nitrogen (5 cycles)
  3. customThe reaction flask was evacuated
  4. custompurged with nitrogen (5 cycles)
  5. filtrationthe mixture was filtered through diatomaceous earth with ethyl acetate (50 mL) and methanol (50 mL) rinses
  6. concentrationThe filtrate was concentrated under vacuum
  7. dissolutionthe residue was dissolved in N,N-dimethylformamide (8 mL)
  8. stirringthe solution was stirred at room temperature for 3 hours
  9. extractionextracted with ethyl acetate (2×50 mL)
  10. washThe combined extracts were washed successively with 1 N NaOH (50 mL) and brine (40 mL)
  11. concentrationconcentrated under vacuum
  12. customThe residue was purified by flash chromatography (SiO2 eluted with CH2Cl2—CH3OH, 100:0-95:5)

Sources & evidence

ORD record
ord-ce553f1cd76b44c98fc2b8cb8253ad6e
Source dataset
uspto-grants-2015_09
Patent number
US09133206B2

Reaction notes

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