Urea → HCID 178517412, compound
Reaction equation
[NH2:1][C:2]1[C:9]([F:10])=[CH:8][C:7]([Br:11])=[CH:6][C:3]=1[CH:4]=O.[NH2:12][C:13](N)=[O:14]>>[Br:11][C:7]1[CH:6]=[C:3]2[C:2](=[C:9]([F:10])[CH:8]=1)[N:1]=[C:13]([OH:14])[N:12]=[CH:4]2Participants
3
Conditions
- Temperature
- 180 °C
Procedure
A stirred mixture of 2-amino-5-bromo-3-fluorobenzaldehyde (2.17 g, 10 mmol) and urea (9 g, 150 mmol) was heated at 180° C. for 2 h. LCMS showed the reaction was completed. The reaction mixture was cooled to RT, and the resulting precipitate was filtered and washed with water (500 mL*3). The moisture trapped was completely removed by the co-evaporation with toluene three times. The title compound (2 g, 83%) was obtained as a yellow solid. MS (ES+) C8H4BrFN2O requires: 242, 244. Found: 243, 245 [M+H]+.
Workup
- temperatureThe reaction mixture was cooled to RT
- filtrationthe resulting precipitate was filtered
- washwashed with water (500 mL*3)
- customThe moisture trapped was completely removed by the co-evaporation with toluene three times
Sources & evidence
- ORD record
- ord-f10c3ae53ac64a69906de1564310ec37
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09126951B2
Reaction notes
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