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Diisopropylethylamine → (R)-ethyl 4-(3'-chlorobiphenyl-4-yl)-3-(2-(ethoxycarbonylamino)acetamido)butanoate

HRID 881821
Notes
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Reaction equation

HRID 881821 reaction equation
Cl.[NH2:2][C@H:3]([CH2:10][C:11]1[CH:16]=[CH:15][C:14]([C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([Cl:23])[CH:18]=2)=[CH:13][CH:12]=1)[CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6].[CH2:24]([O:26][C:27]([NH:29][CH2:30][C:31](O)=[O:32])=[O:28])[CH3:25].CCN=C=NCCCN(C)C.Cl.CCN(C(C)C)C(C)C.C1C=NC2N(O)N=NC=2C=1>CN(C=O)C.O>[Cl:23][C:19]1[CH:18]=[C:17]([C:14]2[CH:15]=[CH:16][C:11]([CH2:10][C@@H:3]([NH:2][C:31](=[O:32])[CH2:30][NH:29][C:27]([O:26][CH2:24][CH3:25])=[O:28])[CH2:4][C:5]([O:7][CH2:8][CH3:9])=[O:6])=[CH:12][CH:13]=2)[CH:22]=[CH:21][CH:20]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 5

HCID 81531DiisopropylethylamineHCID 96472Glycine, N-(ethoxycarbonyl)-HCID 181649HOAtHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 86648190(R)-ethyl 3-amino-4-(3'-chlorobiphenyl-4-yl)butanoate hydrochloride

Product 1

HCID 59607590
(R)-ethyl 4-(3'-chlorobiphenyl-4-yl)-3-(2-(ethoxycarbonylamino)acetamido)butanoate
Yield 73.8%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6228DimethylformamideSolvent

Procedure

A mixture of (R)-ethyl 3-amino-4-(3′-chlorobiphenyl-4-yl)butanoate hydrochloride (173 mg, 0.488 mmol), 2-(ethoxycarbonylamino)acetic acid (86 mg, 0.488 mmol), EDCl (140 mg, 0.732 mmol), DIPEA (0.128 ml, 0.732 mmol) and HOAt (100 mg, 0.732 mmol) in DMF (2.5 ml) is allowed to stir at room temperature for 1 hour. The reaction mixture is diluted with water, and then the precipitated solid is collected on a funnel, washed with H2O, and dried under reduced pressure to give crude. The obtained residue is purified by silica gel flash column chromatography (heptane/EtOAc=100:0 to 0:100) to give (R)-ethyl 4-(3′-chlorobiphenyl-4-yl)-3-(2-(ethoxycarbonylamino)acetamido)butanoate (161 mg); HPLC retention time=1.16 minutes (condition B); MS (m+1)=447.3; 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.25 (t, J=7.07 Hz, 3 H) 1.29 (t, J=7.07 Hz, 3 H) 2.50 (A of ABX, Jab=16.2 Hz, Jax=5.3 Hz, 1 H) 2.54 (B of ABX, Jab=16.2 Hz, Jbx=5.3 Hz, 1 H) 2.89 (A of ABX, Jab=13.6 Hz, Jax=7.8 Hz, 1 H) 2.99 (B of ABX, Jab=13.6 Hz, Jbx=6.6 Hz, 1 H) 3.80 (be d, J=5.8 Hz, 2 H) 4.12-4.23 (m, 4 H) 4.48-4.56 (m, 1 H) 5.15 (br s, 1 H) 6.64 (br d, J=8.8 Hz, 1 H) 7.25-7.27 (m, 2 H) 7.29-7.38 (m, 2 H) 7.43-7.46 (m, 1 H) 7.49-7.52 (m, 2 H) 7.55-7.56 (m, 1 H).

Workup

  1. customthe precipitated solid is collected on a funnel
  2. washwashed with H2O
  3. customdried under reduced pressure
  4. customto give crude
  5. customThe obtained residue is purified by silica gel flash column chromatography (heptane/EtOAc=100:0 to 0:100)

Sources & evidence

ORD record
ord-2fc36b118fac443eb3e94fe806d7613e
Source dataset
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08993631B2

Reaction notes

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