Chloroacetonitrile → HCID 178511314, compound

HRID 2184584Notes

Reaction equation

HRID 2184584 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]=1

Participants

5

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

  1. temperatureThe suspension was warmed
  2. temperatureto reflux for 22.5 hours
  3. filtrationsubsequently filtered
  4. washThe remaining solids were washed with DCM
  5. concentrationthe combined filtrates were concentrated
  6. dissolutionThe resulting brown oil was dissolved into EtOAc
  7. washwashed with water
  8. dry with materialThe organic phase was dried (MgSO4)
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customto give a brown solid which
  12. customflushed through alumina with DCM
  13. concentrationThe eluent was concentrated

Sources & evidence

ORD record
ord-e51e7bf4bf4c4c11ade2aba39499ef84
Source dataset
uspto-grants-2002_06
Patent number
USRE037729E1

Reaction notes

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