HCID 86675689, compound → HCID 71208092, compound

HRID 1622275Notes

Reaction equation

HRID 1622275 reaction equation
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:12]=[C:13]3[CH2:19][C@:18]([CH:21]4[CH2:26][CH2:25][N:24]([C:27]#[N:28])[CH2:23][CH2:22]4)([CH3:20])[O:17][C:14]3=[CH:15][N:16]=2)=[CH:7][CH:6]=1)(=[O:4])=[O:3].[OH:29][NH:30][C:31](=N)[C:32]([CH3:35])([CH3:34])[CH3:33]>>[C:32]([C:31]1[N:28]=[C:27]([N:24]2[CH2:23][CH2:22][CH:21]([C@@:18]3([CH3:20])[O:17][C:14]4=[CH:15][N:16]=[C:11]([C:8]5[CH:9]=[CH:10][C:5]([S:2]([CH3:1])(=[O:3])=[O:4])=[CH:6][CH:7]=5)[CH:12]=[C:13]4[CH2:19]3)[CH2:26][CH2:25]2)[O:29][N:30]=1)([CH3:35])([CH3:34])[CH3:33]

Participants

3

Reactant 2

HCID 86675689HCID 86675689, compoundHCID 178446865HCID 178446865, compound

Product 1

HCID 71208092HCID 71208092, compound

Procedure

The title compound is prepared from (S)-4-[5-(4-methanesulfonyl-phenyl)-2-methyl-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carbonitrile (Intermediate 33; the configuration of the stereocenter is arbitrarily assigned) and N-hydroxy-2,2-dimethyl-propionamidine following a procedure analogous to that described in Example 2. LC (method 4): tR=0.93 min; Mass spectrum (ESI+): m/z=497 [M+H]+.

Sources & evidence

ORD record
ord-cb750fad8d944e7f963def092408c16e
Source dataset
uspto-grants-2014_07
Patent number
US08778926B2

Reaction notes

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