Furfural → HCID 178513717, compound
Reaction equation
[NH2:1][C:2]1[NH:6][N:5]=[C:4]([NH:7][C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([Cl:14])[CH:9]=2)[C:3]=1[C:15]([NH2:17])=[O:16].[O:18]1[CH:22]=[CH:21][CH:20]=[C:19]1[CH:23]=O.[BH4-].[Na+]>CCO.N1CCCCC1>[Cl:14][C:10]1[CH:9]=[C:8]([NH:7][C:4]2[C:3]([C:15]([NH2:17])=[O:16])=[C:2]([NH:1][CH2:23][C:19]3[O:18][CH:22]=[CH:21][CH:20]=3)[NH:6][N:5]=2)[CH:13]=[CH:12][CH:11]=1Participants
Procedure
5-amino-3-((3-chlorophenyl)amino)-1H-pyrazole-4-carboxamide (100 mg) was suspended in EtOH (4 mL) and 2-Furaldehyde (1 eq.) and piperidine (1 drop) were added. Stirred at reflux until intermediate was absent (HPLC). After reaction was complete (18 hrs) it was brought to room temperature and filtered to obtain product as a yellow powder. Powder was washed with EtOH. Product was allowed to dry under vacuum for 1 hr. Resulting imine (100 mg) was suspended in 5 mL MeOH and sodium borohydride (10 eq.) was added. HPLC confirmed reaction was complete (absence of imine). After completion (1 hr), precipitate was filtered to obtain D96 as a light yellow powder. Product was washed with deionized water to remove excess sodium borohydride. Product was allowed to dry under vacuum for 18 hrs. 40 mg (38% yield) of final product was obtained.
Workup
- temperatureat reflux until intermediate
- customAfter reaction
- custom(18 hrs) it
- customwas brought to room temperature
- filtrationfiltered
- customto obtain product as a yellow powder
- washPowder was washed with EtOH
- customto dry under vacuum for 1 hr
- customreaction
- filtrationAfter completion (1 hr), precipitate was filtered
- customto obtain D96 as a light yellow powder
- washProduct was washed with deionized water
- customto remove excess sodium borohydride
- customto dry under vacuum for 18 hrs
Sources & evidence
- ORD record
- ord-8190ba5e787e45e998adce521a068db1
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09346792B2
Reaction notes
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