Ethylenediamine → HCID 71285803, compound

HRID 246195Notes

Reaction equation

HRID 246195 reaction equation
[F:1][CH:2]([F:38])[O:3][CH2:4][C@@H:5]([NH:7][C:8]([C:10]1[C:18]2[C:13](=[N:14][CH:15]=[C:16]([C:19]3[C:27]4[C:22](=[CH:23][C:24]([F:28])=[CH:25][CH:26]=4)[N:21]([CH3:29])[N:20]=3)[N:17]=2)[N:12](COCC[Si](C)(C)C)[CH:11]=1)=[O:9])[CH3:6].C(O)(C(F)(F)F)=O.C(N)CN>ClCCl>[F:38][CH:2]([F:1])[O:3][CH2:4][C@@H:5]([NH:7][C:8]([C:10]1[C:18]2[C:13](=[N:14][CH:15]=[C:16]([C:19]3[C:27]4[C:22](=[CH:23][C:24]([F:28])=[CH:25][CH:26]=4)[N:21]([CH3:29])[N:20]=3)[N:17]=2)[NH:12][CH:11]=1)=[O:9])[CH3:6]

Participants

5

Reactant 3

HCID 3301EthylenediamineHCID 6422Trifluoroacetic acidHCID 712860132-(6-fluoro-1-methyl-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((S)-2-difluoromethoxy-1-methyl-ethyl)-amide

Product 1

HCID 71285803HCID 71285803, compoundYield 32%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

In a 10 mL round-bottom flask, 2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5-(2-trimethylsilanyl-ethoxymethyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((S)-2-difluoromethoxy-1-methyl-ethyl)-amide (10 mg, 0.018 mmol) and TFA (0.5 ml, 6.5 mmol) were combined with dichloromethane (1.5 ml) to give an orange solution. The reaction mixture was stirred at room temperature for 2.5 h then concentrated under reduced pressure. The resultant crude solid was dissolved in dichloromethane (1 mL) and ethylenediamine (30 ul, 0.46 mmol) was added. The reaction mixture was stirred at room temperature for 18 h then concentrated and the residue was precipitated with water. The suspension was stirred for 1 h and the crude solid collected by filtration. The crude solid was purified by trituration (dichloromethane) to afford 2 mg (32%) of 2-(6-fluoro-1-methyl-1H-indazol-3-yl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid ((S)-2-difluoromethoxy-1-methyl-ethyl)-amide as an off-white solid. MS: [M+H]+=419; 1H NMR (300 MHz, DMSO-d6) δ: 12.86 (br. s., 1H), 9.11 (s, 1H), 8.47 (s, 1H), 8.49 (dd, J=9.1, 5.3 Hz, 1H), 8.19 (d, J=8.3 Hz, 1H), 7.70 (dd, J=9.8, 2.3 Hz, 1H), 7.15 (td, J=9.2, 2.1 Hz, 1H), 6.70 (t, J=75.2 Hz, 1H), 4.36-4.54 (m, 1H), 4.16 (s, 3H), 4.00 (d, J=4.5 Hz, 2H), 1.37 (d, J=6.8 Hz, 3H).

Workup

  1. customto give an orange solution
  2. concentrationthen concentrated under reduced pressure
  3. dissolutionThe resultant crude solid was dissolved in dichloromethane (1 mL)
  4. stirringThe reaction mixture was stirred at room temperature for 18 h
  5. concentrationthen concentrated
  6. customthe residue was precipitated with water
  7. stirringThe suspension was stirred for 1 h
  8. filtrationthe crude solid collected by filtration
  9. customThe crude solid was purified by trituration (dichloromethane)

Sources & evidence

ORD record
ord-1fb550d24a5f46e788e8f099cbe3beb8
Source dataset
uspto-grants-2014_02
Patent number
US08658646B2

Reaction notes

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