2-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline → HCID 66779773, compound

HRID 1470387Notes

Reaction equation

HRID 1470387 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]([O:17][CH3:18])=[C:13]([O:19][CH3:20])[CH:12]=3)[O:10][C:3]=12.[CH3:21][C:22]1[C:28](B2OC(C)(C)C(C)(C)O2)=[CH:27][CH:26]=[CH:25][C:23]=1[NH2:24]>>[CH3:20][O:19][C:13]1[CH:12]=[C:11]([C:9]2[O:10][C:3]3[C:4](=[N:5][CH:6]=[CH:7][C:2]=3[C:28]3[C:22]([CH3:21])=[C:23]([CH:25]=[CH:26][CH:27]=3)[NH2:24])[CH:8]=2)[CH:16]=[CH:15][C:14]=1[O:17][CH3:18]

Participants

3

Reactant 2

HCID 467380052-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 66779655HCID 66779655, compound

Product 1

HCID 66779773HCID 66779773, compound

Procedure

The compound was synthesized according to the procedure K using 7-chloro-2-(3,4-dimethoxyphenyl)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-0ed3eae19e374ce5966c364aa0828898
Source dataset
uspto-grants-2015_04
Patent number
US09006440B2

Reaction notes

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