2-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline → HCID 86694440, compound

HRID 1470392Notes

Reaction equation

HRID 1470392 reaction equation
Cl[C:2]1[CH:7]=[CH:6][N:5]=[C:4]2[CH:8]=[C:9]([C:11]3[CH:16]=[CH:15][C:14]([C:17]([N:19]4[CH2:23][CH2:22][CH2:21][CH2:20]4)=[O:18])=[CH:13][CH:12]=3)[O:10][C:3]=12.[CH3:24][C:25]1[C:31](B2OC(C)(C)C(C)(C)O2)=[CH:30][CH:29]=[CH:28][C:26]=1[NH2:27]>>[CH3:24][C:25]1[C:31]([C:2]2[CH:7]=[CH:6][N:5]=[C:4]3[CH:8]=[C:9]([C:11]4[CH:16]=[CH:15][C:14]([C:17]([N:19]5[CH2:23][CH2:22][CH2:21][CH2:20]5)=[O:18])=[CH:13][CH:12]=4)[O:10][C:3]=23)=[CH:30][CH:29]=[CH:28][C:26]=1[NH2:27]

Participants

3

Reactant 2

HCID 467380052-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 66779732HCID 66779732, compound

Product 1

HCID 86694440HCID 86694440, compound

Procedure

The compound was synthesized according to the procedure K using 7-chloro-2-[4-(pyrrolidin-1-ylcarbonyl)phenyl]furo[3,2-b]pyridine and 2-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline.

Workup

  1. customThe compound was synthesized

Sources & evidence

ORD record
ord-35112cb3fd3948f288adb0d1713307f8
Source dataset
uspto-grants-2015_04
Patent number
US09006440B2

Reaction notes

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