Trifluoroacetic acid → 1233182-30-3

HRID 1262357Notes

Reaction equation

HRID 1262357 reaction equation
[CH3:1][S:2][C:3]1[N:8]=[CH:7][C:6]2=[CH:9][CH:10]=[C:11]([C:12]3[N:13](CCC#N)[CH:14]=[CH:15][CH:16]=3)[N:5]2[N:4]=1.C(O)(C(F)(F)F)=O>C(Cl)Cl>[CH3:1][S:2][C:3]1[N:8]=[CH:7][C:6]2=[CH:9][CH:10]=[C:11]([C:12]3[NH:13][CH:14]=[CH:15][CH:16]=3)[N:5]2[N:4]=1

Participants

4

Reactant 2

HCID 6422Trifluoroacetic acidHCID 66711968HCID 66711968, compound

Product 1

HCID 1361634081233182-30-3

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

3-[2-(2-Methylsulfanyl-pyrrolo[2,1-f][1,2,4]triazin-7-yl)-pyrrol-1-yl]-propionitrile: The above bis-TFA salt (92 mg) was taken up in DCM and washed with dilute, aqueous, NaOH. The organic layer was dried by passing through a plug of Na2SO4 and solvent evaporated to yield 2-methylsulfanyl-7-(1H-pyrrol-2-yl)-pyrrolo[2,1-f][1,2,4]triazine (46 mg, 0.20 mmol) which was taken up in acetonitrile (1.0 mL) and treated with 2-propenenitrile (19 uL, 0.29 mmol) and Triton B (5 μL). The mixture was stirred at RT for 1 h. The reaction was taken up in EtOAc and washed with water and brine. The organic layer was dried by passing through a plug of Na2S0. Solvent was removed by rotary evaporation and the resulting residue was triturated with ether (2×2 mL) to yield 44 mg (78%) of product. HPLC RT: 2.93 min; LC/MS: 284 (M+H); 1H NMR (DMSO-d6): 8.99 (s, 1H), 7.13 (m, 1H), 7.09 (s, 2H), 6.66 (dd, J=3.8, 1.7, 1H), 6.27 (dd, J=3.8, 2.9, 1H), 4.30 (t, J=6.6, 2H), 2.86 (t, 2H, J=6.6), —SMe singlet presumably under DMSO peak.

Workup

  1. washwashed
  2. additionwith dilute
  3. customThe organic layer was dried
  4. customevaporated

Sources & evidence

ORD record
ord-32dd2394bc6d4f188fda66bd990ebf7a
Source dataset
uspto-grants-2013_06
Patent number
US08471005B2

Reaction notes

Loading…