Triethylamine → (S)-5-Biphenyl-4-ylmethyl-1-triethylsilanyl-pyrrolidin-2-one

HRID 1500435Notes

Reaction equation

HRID 1500435 reaction equation
[C:1]1([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:6]=[CH:5][C:4]([CH2:7][C@H:8]2[NH:12][C:11](=[O:13])[CH2:10][CH2:9]2)=[CH:3][CH:2]=1.C(N(CC)CC)C.[CH2:27]([Si:29]([CH2:33][CH3:34])([CH2:31][CH3:32])Cl)[CH3:28]>C1COCC1>[C:1]1([C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH:2]=[CH:3][C:4]([CH2:7][C@H:8]2[N:12]([Si:29]([CH2:33][CH3:34])([CH2:31][CH3:32])[CH2:27][CH3:28])[C:11](=[O:13])[CH2:10][CH2:9]2)=[CH:5][CH:6]=1

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 13819ChlorotriethylsilaneHCID 58160438(S)-5-[(Biphenyl-4-yl)methyl]pyrrolidin-2-one

Product 1

HCID 66739229(S)-5-Biphenyl-4-ylmethyl-1-triethylsilanyl-pyrrolidin-2-one

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

A dry flask is charged with 1.256 g (5 mmol) (S)-5-biphenyl-4-ylmethylpyrrolidin-2-one (1-a, R1=H) and 15 ml dry THF. To the resulting clear solution, 2.02 g (20 mmol) triethylamine is added followed by 904 mg (6 mmol) triethylchlorosilane (TES-Cl). The reaction mixture is stirred at room temperature for 4 h and then quenched on addition of 5 ml saturated NaHCO3 solution, 10 ml water and 10 ml isopropyl acetate. The layers are separated and the aqueous layer extracted with 10 ml isopropyl acetate. The combined organic layers are dried over MgSO4, filtered and evaporated. The resulting residue is purified by column chromatography (dichloromethane+1% v/v triethylamine) to give (S)-5-Biphenyl-4-ylmethyl-1-triethylsilanyl-pyrrolidin-2-one (1-a, R1=TES) as a yellow oil. NMR (300 MHz, DMSO-d6, /ppm): 7.63 (m, 4H); 7.55 (m, 2H); 7.32 (m, 3H); 3.80 (m, 1H); 2.85 (m, 1H), 2.70 (m, 1H), 2.10-1.70 (m, 4H), 1.02-0.80 (m, 15H). MS (ESI, m/e) 366 [M+H]+; 731 [2M+H]+. IR (solution in CH2Cl2, /cm−1): 3426; 3047; 2957; 1698; 1672; 1487; 1378; 1242; 1114; 1008.

Workup

  1. customquenched on addition of 5 ml saturated NaHCO3 solution, 10 ml water and 10 ml isopropyl acetate
  2. customThe layers are separated
  3. extractionthe aqueous layer extracted with 10 ml isopropyl acetate
  4. dry with materialThe combined organic layers are dried over MgSO4
  5. filtrationfiltered
  6. customevaporated
  7. customThe resulting residue is purified by column chromatography (dichloromethane+1% v/v triethylamine)

Sources & evidence

ORD record
ord-5e13033bfbfe4a90bc2c234ccfd2733a
Source dataset
uspto-grants-2015_12
Patent number
US09206116B2

Reaction notes

Loading…