Hydrochloric Acid → HCID 178464639, compound

HRID 2273961Notes

Reaction equation

HRID 2273961 reaction equation
[CH2:1]([NH:3][C:4]([N:21]1[CH2:25][CH:24]([CH2:26][CH3:27])[CH:23]=[N:22]1)=[N:5][S:6]([C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[N:14](C(=O)C)[CH2:13][CH2:12]2)(=[O:8])=[O:7])[CH3:2].Cl.C([O-])(O)=O.[Na+]>CCO>[CH2:1]([NH:3][C:4]([N:21]1[CH2:25][CH:24]([CH2:26][CH3:27])[CH:23]=[N:22]1)=[N:5][S:6]([C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[NH:14][CH2:13][CH2:12]2)(=[O:7])=[O:8])[CH3:2]

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 178464638HCID 178464638, compound

Product 1

HCID 178464639HCID 178464639, compoundYield 43%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

1.74 g 1-acetyl-2,3-dihydro-1H-indole-5-sulfonic acid ethylamino-(4-ethyl-4,5-dihydro-pyrazol-1-yl)-methyleneamide was dissolved in 100 mL EtOH, and 22.2 mL of 1M HCl was added. The mixture was stirred for 5 h. under reflux. After cooling to room temperature, the mixture was basified with a 5% NaHCO3 solution and extracted twice with DCM. The combined organic layers were dried over Na2SO4 and evaporated to dryness. The residue was purified by flash chromatography (DCM→DCM/EA 4:1) to give 0.66 g (43%) of 2,3-Dihydro-1H-indole-5-sulfonic acid ethylamino-(4-ethyl-4,5-dihydro-pyrazol-1-yl)-methyleneamide as a yellow oil. 1H NMR (400 MHz, CDCl3) δ 0.97 (t, J=7.52 Hz, 3H), 1.15 (t, J=7.22 Hz, 3H), 1.44-1.68 (m, 2H), 2.97-3.13 (m, 3H), 3.42-3.54 (m, 2H), 3.58-3.72 (m, 3H), 3.99-4.09 (m, 1H), 6.55 (d, J=8.13 Hz, 1H), 6.88 (d, J=1.50 Hz, 1H), 7.00 (br.s., 1H), 7.55-7.65 (m, 2H) [NH invisible].

Workup

  1. temperatureunder reflux
  2. extractionextracted twice with DCM
  3. dry with materialThe combined organic layers were dried over Na2SO4
  4. customevaporated to dryness
  5. customThe residue was purified by flash chromatography (DCM→DCM/EA 4:1)

Sources & evidence

ORD record
ord-35ff7d2789b7428bb19f491f12969dfa
Source dataset
uspto-grants-2015_09
Patent number
US09126942B2

Reaction notes

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