Acetic Acid → HCID 178419476, compound
Reaction equation
[Br:1][C:2]1[S:3][C:4]([C:8]([NH2:10])=O)=[C:5]([Br:7])[N:6]=1.C1(C)C=CC=CC=1.C[N:19]([CH:21](OC)OC)C.C(O)(=O)C.[NH2:30]N.C([O-])(O)=O.[Na+]>CCOC(C)=O.CCCCCC>[Br:1][C:2]1[S:3][C:4]([C:8]2[NH:10][CH:21]=[N:19][N:30]=2)=[C:5]([Br:7])[N:6]=1Participants
Reactant 6
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
To the suspension of 2,4-dibromo-1,3-thiazole-5-carboxamide (0.110 g, 0.385 mmol) in dry Toluene (8.0 mL, 75 mmol) was added DMFDMA (0.204 mL, 1.54 mmol). The mixture was stirred at 60° C. under N2 atmosphere for 3 hours. The solvent was removed and to the intermediate was added acetic acid (2.0 mL, 35 mmol), followed by hydrazine (0.0604 mL, 1.92 mmol). The mixture was heated to 120° C. for 30 min. The mixture was cooled to room temperature, solvent was removed and the residual acetic acid was azeotroped with toluene (2×5 mL) to give an oily material, which was basified with saturated aqueous NaHCO3 to pH˜8 and extracted with EtOAc (3×30 mL). The EtOAc layer was washed with water, brine, dried over Na2SO4, filtered, and evaporated to give a crude product. Chromatography on a silica column using EtOAc/hexane (0/100 to 50/50) gave a solid product (0.073 g, 61%). LCMS: (FA) ES+ 311 and ES− 309.111 NMR (400 MHz, d4-Methanol) 8.53 (s, 1H).
Workup
- customThe solvent was removed and to the intermediate
- temperatureThe mixture was heated to 120° C. for 30 min
- temperatureThe mixture was cooled to room temperature
- customsolvent was removed
- customthe residual acetic acid was azeotroped with toluene (2×5 mL)
- customto give an oily material, which
- extractionextracted with EtOAc (3×30 mL)
- washThe EtOAc layer was washed with water, brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- customevaporated
- customto give a crude product
Sources & evidence
- ORD record
- ord-808f767eb72c474c9432dafa2dd40551
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09139589B2
Reaction notes
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