Water → N-(4-{[bis-(3-methyl-pyridin-2-ylmethyl)-amino]-methyl}-3-hydroxymethyl-benzyl)-methanesulfonamide

HRID 251244Notes

Reaction equation

HRID 251244 reaction equation
C[O:2][C:3](=O)[C:4]1[CH:9]=[C:8]([CH2:10][NH:11][S:12]([CH3:15])(=[O:14])=[O:13])[CH:7]=[CH:6][C:5]=1[CH2:16][N:17]([CH2:26][C:27]1[C:32]([CH3:33])=[CH:31][CH:30]=[CH:29][N:28]=1)[CH2:18][C:19]1[C:24]([CH3:25])=[CH:23][CH:22]=[CH:21][N:20]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3].O>C1COCC1>[CH3:33][C:32]1[C:27]([CH2:26][N:17]([CH2:16][C:5]2[CH:6]=[CH:7][C:8]([CH2:10][NH:11][S:12]([CH3:15])(=[O:14])=[O:13])=[CH:9][C:4]=2[CH2:3][OH:2])[CH2:18][C:19]2[C:24]([CH3:25])=[CH:23][CH:22]=[CH:21][N:20]=2)=[N:28][CH:29]=[CH:30][CH:31]=1

Participants

5

Reactant 3

HCID 962WaterHCID 21226445Aluminium lithium hydrideHCID 672728122-{[Bis-(3-methyl-pyridin-2-ylmethyl)-amino]-methyl}-5-(methanesulfonylamino-methyl)-benzoic acid methyl ester

Product 1

HCID 58997093N-(4-{[bis-(3-methyl-pyridin-2-ylmethyl)-amino]-methyl}-3-hydroxymethyl-benzyl)-methanesulfonamideYield 81%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Under N2, To a solution of 2-{[bis-(3-methyl-pyridin-2-ylmethyl)-amino]-methyl}-5-(methanesulfonylamino-methyl)-benzoic acid methyl ester (0.217 g, 0.450 mmol) in THF (20 mL) was added LiAlH4 (1.0 M in THF, 0.67 mL, 0.67 mmol) at −78° C. After the addition the reaction mixture was brought to room temperature and stirred at room temperature for 30 min. H2O (10 mL) was added, and THF removed. The aqueous residue was extracted with CH2Cl2 (3×20 mL), and the extracts were combined and dried over Na2SO4. After filtration the solvent was removed, and the residue was purified on silica gel column (500:25:1 CH2Cl2/MeOH/NH4OH), affording a white foam (0.165 g, 81%). 1H NMR (CDCl3) δ 2.13 (s, 6H), 2.87 (s, 3H), 3.71 (s, 4H), 3.90 (s, 2H), 4.25 (s, br, 2H), 4.28 (d, 2H, J=6.0 Hz), 4.59 (t, 1H, J=60 Hz), 6.65 (s, br, 1H), 7.06 (dd, 2H, J=4.8, 7.8 Hz), 7.21 (dd, 1H, J=1.5, 7.8 Hz), 7.26-7.31 (m, 2H), 7.38 (d, 2H, J=7.8 Hz), 8.35 (d, 2H, J=4.8 Hz); 13C NMR (CDCl3) δ 18.26, 41.00, 46.84, 57.30, 58.68, 62.79, 122.60, 127.04, 130.68, 131.99, 133.12, 136.72, 137.03, 138.30, 142.35, 146.18, 155.87. ES-MS m/z 455 (M+H). Anal. Calcd. for C24H30N4O3S.0.21CH2Cl2: C, 61.55; H, 6.49; N, 11.86; S, 6.79. Found: C, 61.62; H, 6.58; N, 11.64; S, 6.77.

Workup

  1. additionAfter the addition the reaction mixture
  2. customwas brought to room temperature
  3. customTHF removed
  4. extractionThe aqueous residue was extracted with CH2Cl2 (3×20 mL)
  5. dry with materialdried over Na2SO4
  6. filtrationAfter filtration the solvent
  7. customwas removed
  8. customthe residue was purified on silica gel column (500:25:1 CH2Cl2/MeOH/NH4OH)

Sources & evidence

ORD record
ord-c58069c0e2064ca683db2e525169255d
Source dataset
uspto-grants-2011_01
Patent number
US07863293B2

Reaction notes

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