HCID 60722575, compound → HCID 67632832, compound

HRID 1468033Notes

Reaction equation

HRID 1468033 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].[NH:22]1[C:30]2[C:25](=[CH:26][C:27]([C:31]([N:33]3[CH2:37][CH2:36][CH2:35][CH2:34]3)=[O:32])=[CH:28][CH:29]=2)[CH:24]=[CH:23]1>>[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:22]3[C:30]4[C:25](=[CH:26][C:27]([C:31]([N:33]5[CH2:37][CH2:36][CH2:35][CH2:34]5)=[O:32])=[CH:28][CH:29]=4)[CH:24]=[CH:23]3)=[CH:19][CH:20]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 60722575HCID 60722575, compoundHCID 86696180Tert-butyl 4-((6-chloropyridin-3-yl)oxy)piperidine-1-carboxylate

Product 1

HCID 67632832HCID 67632832, 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 (1H-indol-5-yl)(pyrrolidin-1-yl)methanone (intermediate-18).

Sources & evidence

ORD record
ord-0af9e309077841bc88ecd1c73d57221e
Source dataset
uspto-grants-2015_04
Patent number
US09000175B2

Reaction notes

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