5-(4-Chloro-phenyl)-2-ethynyl-pyridine → HCID 57845330, compound

HRID 734836Notes

Reaction equation

HRID 734836 reaction equation
I[C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][N:11]2[CH2:16][CH2:15][CH:14]([CH3:17])[CH2:13][CH2:12]2)=[C:4]([CH3:18])[CH:3]=1.[Cl:19][C:20]1[CH:25]=[CH:24][C:23]([C:26]2[CH:27]=[CH:28][C:29]([C:32]#[CH:33])=[N:30][CH:31]=2)=[CH:22][CH:21]=1>>[Cl:19][C:20]1[CH:21]=[CH:22][C:23]([C:26]2[CH:27]=[CH:28][C:29]([C:32]#[C:33][C:2]3[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][N:11]4[CH2:16][CH2:15][CH:14]([CH3:17])[CH2:13][CH2:12]4)=[C:4]([CH3:18])[CH:3]=3)=[N:30][CH:31]=2)=[CH:24][CH:25]=1

Participants

3

Procedure

The product was obtained analogously to Example 7.1e starting from 1-[3-(4-iodo-2-methylphenyl)propyl]-4-methylpiperidine and 5-(4-chlorophenyl)-2-ethynylpyridine. Yield: 29 mg (9% of theoretical); C29H31ClN2 (M=443.023); calc.: molpeak (M+H)+: 443/445 (Cl); found: molpeak (M+H)+: 443/445 (Cl); HPLC-MS: 8.55 minutes (method A).

Workup

  1. customThe product was obtained analogously to Example 7.1e
  2. custom8.55 minutes (method A)

Sources & evidence

ORD record
ord-962284b13a4b40a1ad3587905919dc93
Source dataset
uspto-grants-2009_09
Patent number
US07592358B2

Reaction notes

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