4-(4-Piperidinyl)cyclohexanecarboxylic acid → 4-{1-[(S)-4-(2,3-Dihydro-[1,4]dioxino[2,3-b]pyridin-3-yl)-benzyl]-piperidin-4-yl}-cyclohexanecarboxylic acid
Reaction equation
C(OC(N1[CH2:13][CH2:12][N:11]([CH2:14][C:15]2[CH:20]=[CH:19][C:18]([C@@H:21]3[O:30][C:25]4=[N:26][CH:27]=[CH:28][CH:29]=[C:24]4[O:23][CH2:22]3)=[CH:17][CH:16]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.N1CC[CH:34]([CH:37]2[CH2:42][CH2:41][CH:40]([C:43]([OH:45])=[O:44])[CH2:39][CH2:38]2)CC1>>[O:23]1[C:24]2[C:25](=[N:26][CH:27]=[CH:28][CH:29]=2)[O:30][C@@H:21]([C:18]2[CH:19]=[CH:20][C:15]([CH2:14][N:11]3[CH2:10][CH2:9][CH:34]([CH:37]4[CH2:42][CH2:41][CH:40]([C:43]([OH:45])=[O:44])[CH2:39][CH2:38]4)[CH2:13][CH2:12]3)=[CH:16][CH:17]=2)[CH2:22]1Participants
3
Reactant 2
Product 1
Procedure
Compound 265 is prepared from Intermediate C and 4-piperidin-4-yl-cyclohexanecarboxylic acid according to General Method H. (LC/MS method 16: ES+ m/z 437.4 [M+H]+, Rt=2.58 min).
Sources & evidence
- ORD record
- ord-a14576443c16447da90528d5d0d0f2b8
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08946203B2
Reaction notes
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