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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634265Generated: October 30, 2026

Sodium Hydroxide → 3-(3-(6-isopropoxypyridin-2-yl)-1H-indol-5-yl)-1,2,4-thiadiazol-5-amine

https://huagongshe.com/reaction/634265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-(3-(6-isopropoxypyridin-2-yl)-1-tosyl-1H-indol-5-yl)-1,2,4-thiadiazol-5-amineHCID 68328244—
Solvent1,4-DioxaneHCID 31275—
Product3-(3-(6-isopropoxypyridin-2-yl)-1H-indol-5-yl)-1,2,4-thiadiazol-5-amineHCID 6832867720.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3-(3-(6-isopropoxypyridin-2-yl)-1-tosyl-1H-indol-5-yl)-1,2,4-thiadiazol-5-amine (0.25 g, 0.49 mmol) in 1,4-dioxane (10 mL) was added 10% aq NaOH (5 mL) and the reaction was heated at 100° C. for 2 h. The reaction was quenched with ice cold H2O to give a pale yellow precipitate. The precipitate was filtered, washed with ice cold H2O and dried under vacuum. The crude product was purified with preparative HPLC (eluent: 30-100% MeCN in H2O with 5 mM NH4OAc) to give 3-(3-(6-isopropoxypyridin-2-yl)-1H-indol-5-yl)-1,2,4-thiadiazol-5-amine (35 mg, 20.2%). MS (ESI, pos. ion) m/z: 352.3 (M+1); 1H NMR (DMSO-d6, 400 MHz): δ 11.65 (brs, 1H), 8.11 (d, J=2.4 Hz, 1H), 7.91 (dd, J=8.4, 1.6 Hz, 1H) 7.85 (brs, 2H), 7.66 (t, J=8, 1H) 7.46 (d, J=8.8, 1H), 7.39 (d, J=7.6, 1H), 6.50 (d, J=8, 1H), 5.58-5.55 (m, 1H), 1.42 (d, J=6 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321756B2
Source datasetuspto-grants-2016_04
ORD IDord-fc1e62e13aec4bb786e73b91cf87b845
Source noteuspto-grants-2016_04