2-Chloro-5-ethylpyrimidine → 2-[1-(5-Ethyl-pyrimidin-2-yl)-piperidin-4-yl]-5-(1-methanesulfonyl-1,2,3,6-tetrahydro-Pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridine

HRID 1622265Notes

Reaction equation

HRID 1622265 reaction equation
[CH3:1][S:2]([N:5]1[CH2:10][CH:9]=[C:8]([C:11]2[CH:12]=[C:13]3[CH2:19][CH:18]([CH:20]4[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]4)[O:17][C:14]3=[CH:15][N:16]=2)[CH2:7][CH2:6]1)(=[O:4])=[O:3].Cl[C:27]1[N:32]=[CH:31][C:30]([CH2:33][CH3:34])=[CH:29][N:28]=1>>[CH2:33]([C:30]1[CH:29]=[N:28][C:27]([N:23]2[CH2:24][CH2:25][CH:20]([CH:18]3[O:17][C:14]4=[CH:15][N:16]=[C:11]([C:8]5[CH2:9][CH2:10][N:5]([S:2]([CH3:1])(=[O:3])=[O:4])[CH2:6][CH:7]=5)[CH:12]=[C:13]4[CH2:19]3)[CH2:21][CH2:22]2)=[N:32][CH:31]=1)[CH3:34]

Participants

3

Reactant 2

HCID 35727632-Chloro-5-ethylpyrimidineHCID 679735035-(1-Methanesulfonyl-1,2,3,6-tetrahydropyridin-4-yl)-2-piperidin-4-yl-2,3-dihydrofuro[2,3-c]pyridine

Product 1

HCID 575245002-[1-(5-Ethyl-pyrimidin-2-yl)-piperidin-4-yl]-5-(1-methanesulfonyl-1,2,3,6-tetrahydro-Pyridin-4-yl)-2,3-dihydro-furo[2,3-c]pyridine

Procedure

The title compound is prepared from 5-(1-methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-2-piperidin-4-yl-2,3-dihydro-furo[2,3-c]pyridine and 2-chloro-5-ethylpyrimidine following a procedure analogous to that described in Example 1. LC (method 5): tR=0.91 min; Mass spectrum (ESI+): m/z=470 [M+H]+.

Sources & evidence

ORD record
ord-5fe57f0eb2ec4209b06cb8ceb9b1f73e
Source dataset
uspto-grants-2014_07
Patent number
US08778926B2

Reaction notes

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