HCID 67215192, compound → HCID 178499189, compound

HRID 2421035Notes

Reaction equation

HRID 2421035 reaction equation
COC1C=CC(C[N:8]2[C:12]([N:13]([CH3:18])[S:14]([CH3:17])(=[O:16])=[O:15])=[C:11]([C:19]([O:21][CH3:22])=[O:20])[N:10]=[N:9]2)=CC=1>FC(F)(F)C(O)=O>[CH3:18][N:13]([S:14]([CH3:17])(=[O:16])=[O:15])[C:12]1[NH:8][N:9]=[N:10][C:11]=1[C:19]([O:21][CH3:22])=[O:20]

Participants

3

Procedure

Methyl 1-(4-methoxybenzyl)-5-[methyl(methylsulfonyl)amino]-1H-1,2,3-triazole-4-carboxylate (0.54 g) was stirred in trifluoroacetic acid (5 mL) at 60° C. for 6 h. The mixture was evaporated and the residue was co-evaporated with toluene. Purification by flash chromatoraphy (1:49 methanol/DCM) gave the subtitle compound as a gum (0.36 g).

Workup

  1. customThe mixture was evaporated
  2. customPurification by flash chromatoraphy (1:49 methanol/DCM)

Sources & evidence

ORD record
ord-870d238d560745c388e5338d467e0db3
Source dataset
uspto-grants-2011_06
Patent number
US07956070B2

Reaction notes

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