3-Bromo-1H-pyrrolo[2,3-c]pyridine → HCID 49832438, compound

HRID 1945792Notes

Reaction equation

HRID 1945792 reaction equation
[CH3:1][N:2]([CH3:38])[CH:3]1[CH2:8][CH2:7][N:6]([CH2:9][C:10]2[S:18][C:17]3[C:16]([N:19]4[CH2:24][CH2:23][O:22][CH2:21][CH2:20]4)=[N:15][C:14]([Sn](CCCC)(CCCC)CCCC)=[N:13][C:12]=3[CH:11]=2)[CH2:5][CH2:4]1.Br[C:40]1[C:48]2[C:43](=[CH:44][N:45]=[CH:46][CH:47]=2)[NH:42][CH:41]=1>>[CH3:1][N:2]([CH3:38])[CH:3]1[CH2:4][CH2:5][N:6]([CH2:9][C:10]2[S:18][C:17]3[C:16]([N:19]4[CH2:20][CH2:21][O:22][CH2:23][CH2:24]4)=[N:15][C:14]([C:40]4[C:48]5[C:43](=[CH:44][N:45]=[CH:46][CH:47]=5)[NH:42][CH:41]=4)=[N:13][C:12]=3[CH:11]=2)[CH2:7][CH2:8]1

Participants

3

Reactant 2

HCID 124108563-Bromo-1H-pyrrolo[2,3-c]pyridineHCID 59605498Dimethyl-[1-(4-morpholin-4-yl-2-(tributylstannanyl)thieno[3,2-d]pyrimidin-6-ylmethyl)piperidin-4-yl]amine

Product 1

HCID 49832438HCID 49832438, compound

Procedure

Following General Procedure G for Stille coupling, N,N-dimethyl-1-((4-morpholino-2-(tributylstannyl)thieno[3,2-d]pyrimidin-6-yl)methyl)piperidin-4-amine and 3-bromo-1H-pyrrolo[2,3-c]pyridine were reacted to give 216. LCMS m/z: 478.6 (MH+)

Workup

  1. customwere reacted

Sources & evidence

ORD record
ord-31a4b191e9b747d3811a0d538e377193
Source dataset
uspto-grants-2013_03
Patent number
US08394796B2

Reaction notes

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