Triethylamine → 2-(3-Methyl-1,2,4-oxadiazol-5-yl)-N-[(1S,2S)-2-{[5-(trifluoromethyl)pyridin-2-yl]amino}cyclopentyl]benzamide

HRID 1750580Notes

Reaction equation

HRID 1750580 reaction equation
[CH3:1][C:2]1[N:6]=[C:5]([C:7]2[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=2[C:9]([OH:11])=O)[O:4][N:3]=1.Cl.[F:17][C:18]([F:33])([F:32])[C:19]1[CH:20]=[CH:21][C:22]([NH:25][C@H:26]2[CH2:30][CH2:29][CH2:28][C@@H:27]2[NH2:31])=[N:23][CH:24]=1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(N(CC)CC)C>CN(C=O)C.CS(C)=O>[CH3:1][C:2]1[N:6]=[C:5]([C:7]2[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=2[C:9]([NH:31][C@H:27]2[CH2:28][CH2:29][CH2:30][C@@H:26]2[NH:25][C:22]2[CH:21]=[CH:20][C:19]([C:18]([F:33])([F:17])[F:32])=[CH:24][N:23]=2)=[O:11])[O:4][N:3]=1

Participants

7

Procedure

A solution of 2-(3-methyl-1,2,4-oxadiazol-5-yl)benzoic acid (CAS number 475105-77-2; 57.4 mg, 0.28 mmol), (1S,2S)-1-N-[5-(trifluoromethyl)pyridin-2-yl]cyclopentane-1,2-diamine hydrochloride (Intermediate 1; 72 mg, 0.26 mmol), HATU (146 mg, 0.38 mmol) and triethylamine (107 μl, 0.77 mmol) in dry DMF (852 μl) was stirred at room temperature for 72 hours. The reaction was diluted with DMSO and filtered through cotton wool before being purified by reverse phase preparative HPLC (eluted with acetonitrile/water containing 0.1% ammonia) to afford the title compound.

Workup

  1. filtrationfiltered through cotton wool
  2. custombefore being purified by reverse phase preparative HPLC (eluted with acetonitrile/water containing 0.1% ammonia)

Sources & evidence

ORD record
ord-c1dcbb6369bb4b2faec139440b4a0aad
Source dataset
uspto-grants-2015_10
Patent number
US09156829B2

Reaction notes

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