tert-Butyl 4-ethynylpiperidine-1-carboxylate → HCID 46892660, compound

HRID 570663Notes

Reaction equation

HRID 570663 reaction equation
[N:1]([CH:4]1[CH2:23][N:8]2[C:9]3[C:14]([C:15]([CH2:16][C:17]([O:19]CCC)=[O:18])=[C:7]2[CH2:6][CH2:5]1)=[CH:13][CH:12]=[CH:11][CH:10]=3)=[N+:2]=[N-:3].[C:24]([CH:26]1[CH2:31][CH2:30][N:29]([C:32]([O:34][C:35]([CH3:38])([CH3:37])[CH3:36])=[O:33])[CH2:28][CH2:27]1)#[CH:25]>>[C:35]([O:34][C:32]([N:29]1[CH2:30][CH2:31][CH:26]([C:24]2[N:1]([CH:4]3[CH2:23][N:8]4[C:9]5[C:14]([C:15]([CH2:16][C:17]([OH:19])=[O:18])=[C:7]4[CH2:6][CH2:5]3)=[CH:13][CH:12]=[CH:11][CH:10]=5)[N:2]=[N:3][CH:25]=2)[CH2:27][CH2:28]1)=[O:33])([CH3:38])([CH3:37])[CH3:36]

Participants

3

Procedure

The title compound was prepared using procedures described in EXAMPLE 3 from propyl (7-azido-6,7,8,9-tetrahydropyrido[1,2-α]indol-10-yl)acetate and tert-butyl 4-ethynylpiperidine-1-carboxylate. MS (+ESI) m/z: 480.2.

Sources & evidence

ORD record
ord-e9a10dd0371c430990b7003ec9991bc7
Source dataset
uspto-grants-2015_05
Patent number
US09023864B2

Reaction notes

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