Chloroacetonitrile → HCID 178511314, compound
Reaction equation
[F:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([CH:11]3[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]3)=[N:7][NH:8]2)=[CH:4][CH:3]=1.Cl[CH2:18][C:19]#[N:20].C(Cl)Cl.CCOC(C)=O>C(#N)C>[F:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([CH:11]3[CH2:16][CH2:15][N:14]([CH2:18][C:19]#[N:20])[CH2:13][CH2:12]3)=[N:7][NH:8]2)=[CH:4][CH:3]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred suspension of 4-(6-fluoro-1H-indazol-3-yl)piperidine (4.95 g, 22.6 mmol) and NaHCOa (2.1 g, 24.9 mmol) in dry acetonitrile (110 ml) was added chloroacetonitrile (1.6 ml, 24.9 mmol) at room temperature, under nitrogen. The suspension was warmed to reflux for 22.5 hours, cooled to room temperature, and subsequently filtered. The remaining solids were washed with DCM and the combined filtrates were concentrated. The resulting brown oil was dissolved into EtOAc and washed with water. The organic phase was dried (MgSO4), filtered and concentrated to give a brown solid which was re-dissolved into DCM/EtOAc and flushed through alumina with DCM. The eluent was concentrated to give 5.2 g of the desired product as a solid, m.p. 149°-151° C. ANALYSIS: Calculated for C14H15FN4 : 65.10%C 5.85%H 21.69%N Found: 64.84%C 5.90%H 21.74%N
Workup
- temperatureThe suspension was warmed
- temperatureto reflux for 22.5 hours
- filtrationsubsequently filtered
- washThe remaining solids were washed with DCM
- concentrationthe combined filtrates were concentrated
- dissolutionThe resulting brown oil was dissolved into EtOAc
- washwashed with water
- dry with materialThe organic phase was dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated
- customto give a brown solid which
- customflushed through alumina with DCM
- concentrationThe eluent was concentrated
Sources & evidence
- ORD record
- ord-c1e7ead3e8a14944a5a29554e2bdd1fb
- Source dataset
- uspto-grants-1997_02
- Patent number
- US05599821
Reaction notes
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