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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518769Generated: October 31, 2026

Dichloromethane → HCID 178457866, compound

https://huagongshe.com/reaction/518769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAmmonium formateHCID 2723923—
ReactantHCID 178457867HCID 178457867—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 178457866HCID 17845786697%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of cis-N-Isopropyl-4-(5-(methylsulfonyl)-2-nitrophenylamino)cyclohexanecarboxamide (0.120 g, 0.313 mmol) in MeOH (1.2 mL) was added 5% Pd/C (0.067 g, 0.031 mmol) and ammonium formate (0.154 mL, 3.13 mmol) (exotherm). The reaction mixture was stirred at 20° C. for 1 hour and then the mixture was filtered through a pad of Celite® brand filter aid, washing with MeOH. The filtrate was concentrated under vacuum, and the remaining residue was dissolved in DCM then washed with water. The organic layer was concentrated under vacuum. The residue was purified by flash chromatography, eluting with 0-80% 90:10:1 DCM/MeOH/NH4OH:DCM to afford cis-4-(2-amino-5-(methylsulfonyl) phenylamino)-N-isopropylcyclohexanecarboxamide as a pale yellow oil (0.107 g, 97% yield). MS (ESI pos. ion) m/z: 354.2 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115127B2
Source datasetuspto-grants-2015_08
ORD IDord-7b2ce9c5a9bf49ebac695dbfae3a358f
Source noteuspto-grants-2015_08