Boron tribromide → HCID 57600208, compound

HRID 1787836Notes

Reaction equation

HRID 1787836 reaction equation
[Br:1][C:2]1[NH:10][C:9]2[C:8](=[O:11])[N:7]3[C:12]([CH2:15][CH2:16][NH:17][C:18](=[O:27])[C:19]4[CH:24]=[CH:23][C:22]([O:25]C)=[CH:21][CH:20]=4)=[N:13][N:14]=[C:6]3[N:5]([CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[C:4]=2[N:3]=1.B(Br)(Br)Br>C(Cl)Cl>[Br:1][C:2]1[NH:10][C:9]2[C:8](=[O:11])[N:7]3[C:12]([CH2:15][CH2:16][NH:17][C:18](=[O:27])[C:19]4[CH:24]=[CH:23][C:22]([OH:25])=[CH:21][CH:20]=4)=[N:13][N:14]=[C:6]3[N:5]([CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[C:4]=2[N:3]=1

Participants

4

Procedure

To a solution of N-[2-(7-bromo-5-oxo-9-pentyl-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-3-yl)ethyl]-4-methoxybenzamide (63.0 mg, 0.125 mmol) in CH2Cl2 (5 mL) at 0° C. was added a solution of Boron tribromide in CH2Cl2 (1.0 M, 1.3 mL, 1.3 mmol). The mixture was stirred at room temperature overnight. The reaction mixture was quenched with water and then concentrated and purified by preparative LCMS to give the desired product. LCMS calculated for C20H23BrN7O3(M+H): m/z=488.1, 490.1; found: 488.0, 489.9.

Workup

  1. customThe reaction mixture was quenched with water
  2. concentrationconcentrated
  3. custompurified by preparative LCMS

Sources & evidence

ORD record
ord-f77f09454d8640f9bf014e4ad2eb415f
Source dataset
uspto-grants-2009_03
Patent number
US07511050B2

Reaction notes

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