1-Hydroxybenzotriazole → tert-Butyl cis(+/-)-3-(4-{[(5-Ethyl-4-trifluoromethyl-1H-imidazol-2-yl)carbonyl]amino}-3-ethoxypiperidin-1-yl)benzoate

HRID 43497Notes

Reaction equation

HRID 43497 reaction equation
[NH2:1][C@H:2]1[CH2:7][CH2:6][N:5]([C:8]2[CH:9]=[C:10]([CH:18]=[CH:19][CH:20]=2)[C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[CH2:4][C@H:3]1[O:21][CH2:22][CH3:23].[CH2:24]([C:26]1[NH:30][C:29]([C:31](O)=[O:32])=[N:28][C:27]=1[C:34]([F:37])([F:36])[F:35])[CH3:25].CCN=C=NCCCN(C)C.Cl.C1C=CC2N(O)N=NC=2C=1>>[CH2:24]([C:26]1[NH:30][C:29]([C:31]([NH:1][C@H:2]2[CH2:7][CH2:6][N:5]([C:8]3[CH:9]=[C:10]([CH:18]=[CH:19][CH:20]=3)[C:11]([O:13][C:14]([CH3:16])([CH3:17])[CH3:15])=[O:12])[CH2:4][C@H:3]2[O:21][CH2:22][CH3:23])=[O:32])=[N:28][C:27]=1[C:34]([F:36])([F:37])[F:35])[CH3:25]

Participants

5

Procedure

The same operation as in Example (1g) was performed using tert-butyl cis(±)-3-(4-amino-3-ethoxypiperidin-1-yl)benzoate obtained in Example (48e) (about 0.22 mmol), 5-ethyl-4-(trifluoromethyl)-1H-imidazole-2-carboxylic acid obtained by the method described in Example (39e) (40 mg, 0.19 mmol), WSC hydrochloride (120 mg, 0.63 mmol) and HOBT (40 mg, 0.30 mmol), to obtain 81.0 mg of the title compound (83%).

Workup

  1. customobtained by the method

Sources & evidence

ORD record
ord-417ca603694f4e8a8690d585d830847f
Source dataset
uspto-grants-2013_09
Patent number
US08536197B2

Reaction notes

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