HCID 178464639, compound → HCID 178464643, compound

HRID 1044692Notes

Reaction equation

[CH2:1]([NH:3][C:4]([N:18]1[CH2:22][CH:21]([CH2:23][CH3:24])[CH:20]=[N:19]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:8])=[O:7])[CH3:2]>C1(C)C=CC=CC=1.[Pd]>[CH2:1]([NH:3][C:4]([N:18]1[CH2:22][CH:21]([CH2:23][CH3:24])[CH:20]=[N:19]1)=[N:5][S:6]([C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[NH:14][CH:13]=[CH:12]2)(=[O:7])=[O:8])[CH3:2]

Participants

Conditions

Temperature: 50 °C

Procedure

0.42 g 2,3-Dihydro-1H-indole-5-sulfonic acid ethylamino-(4-ethyl-4,5-dihydro-pyrazol-1-yl)-methyleneamide was dissolved in 25 mL toluene, and 10 mol % of palladium on carbon was added. The mixture was stirred at 50° C. for 5 days, with addition of fresh catalyst (10 mol %) after 2 days. The mixture was cooled to room temperature and filtered over Hyflo. The filtrate was evaporated to dryness and the residue was purified by flash chromatography (DCM→DCM/EA 9:1) to give 0.26 g (66%) of 1H-Indole-5-sulfonic acid ethylamino-(4-ethyl-4,5-dihydro-pyrazol-1-yl)-methyleneamide as a blue oil. 1H NMR (400 MHz, CDCl3) δ 0.87 (t, J=7.37 Hz, 3H), 1.08 (t, J=7.22 Hz, 3H), 1.32-1.59 (m, 2H), 2.89-3.02 (m, 1H), 3.35-3.50 (m, 2H), 3.58 (dd, J=11.44, 7.52 Hz, 1H), 3.96 (t, J=11.29 Hz, 1H), 6.54-6.58 (m, 1H), 6.85 (d, J=1.50 Hz, 1H), 6.97 (br.s., 1H) 7.23-7.29 (m, 1H), 7.42 (d, J=8.73 Hz, 1H), 7.69 (dd, J=8.73, 1.81 Hz, 1H), 8.24 (d, J=1.20 Hz, 1H), 9.43 (br.s., 1H).

Workup

temperatureThe mixture was cooled to room temperature
filtrationfiltered over Hyflo
customThe filtrate was evaporated to dryness
customthe residue was purified by flash chromatography (DCM→DCM/EA 9:1)

Sources & evidence

ORD record: ord-7da72d25a9e44a49b1546d4df87c7884
Source dataset: uspto-grants-2013_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08563723B2

Reaction notes

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