Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396345Generated: November 1, 2026

Trifluoroacetic acid → HCID 71626820, compound

https://huagongshe.com/reaction/1396345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
Reactant[(1S,2R)-2-(6-carbamoyl-5-p-tolylamino-pyridazin-3-ylamino)-cyclohexyl]-carbamic acid tert-butyl esterHCID 86689714—
SolventDichloromethaneHCID 6344—
ProductAmmonium HydroxideHCID 14923—
ProductHCID 71626820HCID 71626820149.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

[(1S,2R)-2-(6-carbamoyl-5-p-tolylamino-pyridazin-3-ylamino)-cyclohexyl]-carbamic acid tert-butyl ester (26 mg, 0.059 mmol) was dissolved in dichloromethane (0.6 mL) then cooled to 0° C. Trifluoroacetic acid (0.27 mL, 3.54 mmol) was added drop-wise then the reaction mixture was warmed to 25° C. After 4 h, the mixture was cooled in an ice bath and neutralized with sodium bicarbonate solution. The mixture was extracted with ethyl acetate, and the combined organic layers washed with brine, dried (sodium sulfate), filtered, and concentrated in vacuo. Purification by chromatography (silica, 0 to 80% of a 0.1:0.01 solution of methanol:NH4OH in dichloromethane) gave 6-((1R,2S)-2-amino-cyclohexylamino)-4-p-tolylamino-pyridazine-3-carboxylic acid amide (15 mg, 72%) as an off-white solid. 1H NMR (300 MHz, DMSO-d6) δ ppm 10.30 (s, 1H) 8.20-8.30 (m, 1H) 7.44-7.55 (m, 1H) 7.17-7.27 (m, 2H) 7.07-7.17 (m, 2H) 6.59 (d, J=7.9 Hz, 1H) 6.33 (s, 1H) 3.95-4.09 (m, 1H) 2.93-3.06 (m, 1H) 2.30 (s, 3H) 1.19-1.68 (m, 9H); LCMS (EI/CI) m/z: 341 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901124B2
Source datasetuspto-grants-2014_12
ORD IDord-8bb89752b4fb4315859cf914628c6a56
Source noteuspto-grants-2014_12