Diisopropylethylamine → Biphenyl-2-ylcarbamic Acid 1-[2-[(4-{[2-(3-{(R)-2-{(R)-2-(8-Benzyloxy-2-oxo-1,2-dihydroquinolin-5-yl)-2-(tert-butyldimethylsilanyloxy)-ethylamino]propyl}phenyl)ethylcarbamoyl]methyl}phenyl)-methylcarbamoyl]ethyl}piperidin-4-yl Ester

HRID 1039865Notes

Reaction equation

HRID 1039865 reaction equation
[NH2:1][CH2:2][CH2:3][C:4]1[CH:5]=[C:6]([CH2:10][C@H:11]([NH:13][CH2:14][C@@H:15]([C:24]2[CH:33]=[CH:32][C:31]([O:34][CH2:35][C:36]3[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=3)=[C:30]3[C:25]=2[CH:26]=[CH:27][C:28](=[O:42])[NH:29]3)[O:16][Si:17]([C:20]([CH3:23])([CH3:22])[CH3:21])([CH3:19])[CH3:18])[CH3:12])[CH:7]=[CH:8][CH:9]=1.[C:43]1([C:75]2[CH:80]=[CH:79][CH:78]=[CH:77][CH:76]=2)[CH:48]=[CH:47][CH:46]=[CH:45][C:44]=1[NH:49][C:50]([O:52][CH:53]1[CH2:58][CH2:57][N:56]([CH2:59][CH2:60][C:61](CNC2C=CC(CC(O)=O)=CC=2)=[O:62])[CH2:55][CH2:54]1)=[O:51].[O-]S(C(F)(F)F)(=O)=O.C([N:92]([CH2:96]C)[CH:93]([CH3:95])[CH3:94])(C)C>C(Cl)Cl>[CH2:35]([O:34][C:31]1[CH:32]=[CH:33][C:24]([C@@H:15]([O:16][Si:17]([C:20]([CH3:21])([CH3:23])[CH3:22])([CH3:19])[CH3:18])[CH2:14][NH:13][C@H:11]([CH3:12])[CH2:10][C:6]2[CH:5]=[C:4]([CH2:3][CH2:2][NH:1][C:15]([CH2:24][C:25]3[CH:30]=[CH:94][C:93]([N:92]([CH3:96])[C:61]([CH2:60][CH2:59][N:56]4[CH2:57][CH2:58][CH:53]([O:52][C:50](=[O:51])[NH:49][C:44]5[CH:45]=[CH:46][CH:47]=[CH:48][C:43]=5[C:75]5[CH:80]=[CH:79][CH:78]=[CH:77][CH:76]=5)[CH2:54][CH2:55]4)=[O:62])=[CH:95][CH:26]=3)=[O:16])[CH:9]=[CH:8][CH:7]=2)=[C:25]2[C:30]=1[NH:29][C:28](=[O:42])[CH:27]=[CH:26]2)[C:36]1[CH:37]=[CH:38][CH:39]=[CH:40][CH:41]=1

Participants

6

Reactant 4

HCID 81531DiisopropylethylamineHCID 2758875TrifluoromethanesulfonateHCID 667815115-[(R)-2-{(R)-2-[3-(2-Aminoethyl)phenyl]-1-methylethylamino}-1-(tert-butyldimethylsilanyloxy)ethyl]-8-benzyloxy-1H-quinolin-2-oneHCID 66781677[4-({3-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionyl}methylamino)-phenyl]acetic acid

Product 1

HCID 86704962Biphenyl-2-ylcarbamic Acid 1-[2-[(4-{[2-(3-{(R)-2-{(R)-2-(8-Benzyloxy-2-oxo-1,2-dihydroquinolin-5-yl)-2-(tert-butyldimethylsilanyloxy)-ethylamino]propyl}phenyl)ethylcarbamoyl]methyl}phenyl)-methylcarbamoyl]ethyl}piperidin-4-yl EsterYield 76.1%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A mixture of 5-[(R)-2-{(R)-2-[3-(2-aminoethyl)phenyl]-1-methylethylamino}-1-(tert-butyldimethylsilanyloxy)ethyl]-8-benzyloxy-1H-quinolin-2-one (0.586 g, 1.00 mmol); [4-({3-[4-(biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionyl}methylamino)-phenyl]acetic acid (0.516 g, 1.00 mmol); 2-chloropyridium triflate on Wang resin (polymer-supported Mukaiyama reagent) (1.19 mmol/g loading; 1.68 g, 2.00 mmol); and N,N-diisopropylethylamine (522 μL, 3.00 mmol) in DCM (5.00 mL) was stirred at room temperature overnight. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel chromatography (0-5% MeOH in DCM) to give the title compound (412 mg, 38% yield) as an off-white oil.

Workup

  1. filtrationThe reaction mixture was filtered
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. customThe residue was purified by silica gel chromatography (0-5% MeOH in DCM)

Sources & evidence

ORD record
ord-b1ee14bcad0b42959773894e18f47c0e
Source dataset
uspto-grants-2013_10
Patent number
US08551978B2

Reaction notes

Loading…