Toluene → tert-butyl 5-(1-methyl-3-trifluoromethyl-1H-pyrazol-5-yl)thiophene-2-carbamate

HRID 1181259Notes

Reaction equation

HRID 1181259 reaction equation
[CH3:1][N:2]1[C:6]([C:7]2[S:11][C:10](C(O)=O)=[CH:9][CH:8]=2)=[CH:5][C:4]([C:15]([F:18])([F:17])[F:16])=[N:3]1.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:26])C=CC=CC=1.C(C1C=CC=CC=1[N:40]([CH2:43]C)CC)C.C1(C)C=CC=CC=1.[C:56]([OH:60])([CH3:59])([CH3:58])[CH3:57]>>[CH3:1][N:2]1[C:6]([C:7]2[S:11][C:10]([NH:40][C:43]([O:60][C:56]([CH3:59])([CH3:58])[CH3:57])=[O:26])=[CH:9][CH:8]=2)=[CH:5][C:4]([C:15]([F:16])([F:17])[F:18])=[N:3]1

Participants

6

Conditions

Temperature
80 °C

Procedure

5-(1-methyl-3-trifluoromethyl-1H-pyrazol-5-yl)thiophene-2-carboxylic acid, diphenylphosphoryl azide, triethyamline and toluene was stirred at 50° C. for 30 minutes. Then, tert-butanol was added to the reaction solution. After stirring at 80° C. for 5 hours, it was subjected to purification in the usual way to give tert-butyl 5-(1-methyl-3-trifluoromethyl-1H-pyrazol-5-yl)thiophene-2-carbamate as light yellow crystals.

Workup

  1. customit was subjected to purification in the usual way

Sources & evidence

ORD record
ord-fd944739794940a0bb9d31b4de1b25dd
Source dataset
uspto-grants-2007_10
Patent number
US07285554B2

Reaction notes

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