Hydrochloric Acid → Methyl 2-(4-(2-(3-(2-amino-4-methyl-6-(pentylamino)pyrimidin-5-yl)propylamino)-2-oxoethyl)phenyl)acetate

HRID 1617169Notes

Reaction equation

HRID 1617169 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([CH3:8])[C:5]([CH2:9][CH2:10][CH2:11][NH:12][C:13](=[O:25])[CH2:14][C:15]2[CH:20]=[CH:19][C:18]([CH2:21][C:22]([OH:24])=[O:23])=[CH:17][CH:16]=2)=[C:4]([NH:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[N:3]=1.Cl.[CH3:33]O>O1CCOCC1>[NH2:1][C:2]1[N:7]=[C:6]([CH3:8])[C:5]([CH2:9][CH2:10][CH2:11][NH:12][C:13](=[O:25])[CH2:14][C:15]2[CH:20]=[CH:19][C:18]([CH2:21][C:22]([O:24][CH3:33])=[O:23])=[CH:17][CH:16]=2)=[C:4]([NH:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[N:3]=1

Participants

5

Procedure

The product from step (i) was dissolved in MeOH (20 mL) then a solution of HCl in dioxane (4M, 0.3 ml) was added and stirred overnight. Solvent was removed and the residue purified by RPHPLC to afford the title compound, 0.032 g.

Workup

  1. customSolvent was removed
  2. customthe residue purified by RPHPLC

Sources & evidence

ORD record
ord-3864013422a146228a2f5026f75792b8
Source dataset
uspto-grants-2014_07
Patent number
US08765939B2

Reaction notes

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