HCID 59803855, compound → HCID 86696197, compound

HRID 1468022Notes

Reaction equation

HRID 1468022 reaction equation
Cl[C:2]1[N:7]=[CH:6][C:5]([O:8][CH:9]2[CH2:14][CH2:13][N:12]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:11][CH2:10]2)=[CH:4][CH:3]=1.[CH3:22][S:23]([C:26]1[CH:27]=[C:28]2[CH:34]=[CH:33][NH:32][C:29]2=[N:30][CH:31]=1)(=[O:25])=[O:24]>>[C:18]([O:17][C:15]([N:12]1[CH2:13][CH2:14][CH:9]([O:8][C:5]2[CH:6]=[N:7][C:2]([N:32]3[C:29]4=[N:30][CH:31]=[C:26]([S:23]([CH3:22])(=[O:24])=[O:25])[CH:27]=[C:28]4[CH:34]=[CH:33]3)=[CH:3][CH:4]=2)[CH2:10][CH2:11]1)=[O:16])([CH3:21])([CH3:20])[CH3:19]

Participants

3

Reactant 2

HCID 59803855HCID 59803855, compoundHCID 86696180Tert-butyl 4-((6-chloropyridin-3-yl)oxy)piperidine-1-carboxylate

Product 1

HCID 86696197HCID 86696197, compound

Procedure

The title compound was prepared by following the similar procedure as described in Example-1 by using tert-Butyl 4-((6-chloropyridin-3-yl)oxy)piperidine-1-carboxylate (intermediate-6) and 5-(methylsulfonyl)-1H-pyrrolo[2,3-b]pyridine (intermediate-25).

Sources & evidence

ORD record
ord-54809b3bf44646c0a73ba05cacac305d
Source dataset
uspto-grants-2015_04
Patent number
US09000175B2

Reaction notes

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