HCID 67616343, compound → HCID 67616424, compound

HRID 1468019Notes

Reaction equation

HRID 1468019 reaction equation
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([O:14][C:15]2[CH:16]=[N:17][C:18](Cl)=[CH:19][CH:20]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH2:22]([S:24]([C:27]1[CH:28]=[C:29]2[C:33](=[CH:34][CH:35]=1)[NH:32][CH:31]=[CH:30]2)(=[O:26])=[O:25])[CH3:23]>>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([O:14][C:15]2[CH:16]=[N:17][C:18]([N:32]3[C:33]4[C:29](=[CH:28][C:27]([S:24]([CH2:22][CH3:23])(=[O:26])=[O:25])=[CH:35][CH:34]=4)[CH:30]=[CH:31]3)=[CH:19][CH:20]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 67616343HCID 67616343, compoundHCID 86696180Tert-butyl 4-((6-chloropyridin-3-yl)oxy)piperidine-1-carboxylate

Product 1

HCID 67616424HCID 67616424, 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-carboxy late (intermediate-6) and 5-(ethylsulfonyl)-1H-indole (intermediate-81).

Sources & evidence

ORD record
ord-61d8ca04405c4c499b9f8ef17b22111a
Source dataset
uspto-grants-2015_04
Patent number
US09000175B2

Reaction notes

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