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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448119Generated: October 31, 2026

Dichloromethane → HCID 59302970, compound

https://huagongshe.com/reaction/448119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantN,N-dimethylformamide methanolHCID 21901440—
ReactantHCID 59302965HCID 59302965—
ProductHCID 59302970HCID 59302970—

Reaction Conditions

Temperature80 °C

Reaction Steps

A 15 mL pressure vessel was charged with 4-tert-butyl-N-[4-iodo-2-(5-ethyl-4-methyl-4H-[1,2,4]triazol-3-yl)-phenyl]-benzenesulfonamide (prepared according to general procedure C, 551 mg, 1.05 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) complex with CH2Cl2 (1:1) (86 mg, 0.105 mmol), triethylamine (290 μL, 2.1 mmol), and DMF/MeOH (4:1) (5 mL). The vessel was placed under an atmosphere of CO (50 p.s.i.), heated to 80° C., and stirred overnight. The following day, the volatiles were removed in vacuo, the residue dissolved in EtOAc, and the organics washed twice with 1 M HCl. The aqueous solution was then extracted three times with EtOAc. The EtOAc extractions were then pooled together and washed with brine. The organic solvent was then removed and the resultant residue was purified by silica gel chromatography to afford 4-(4-tert-butyl-benzenesulfonylamino)-3-(5-ethyl-4-methyl-4H-[1,2,4]triazol-3-yl)-benzoic acid methyl ester as a yellow foam: MS (ES) M+H expected 457.2, found 457.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481579B2
Source datasetuspto-grants-2013_07
ORD IDord-cb093574a1814adfacadf84cf8f16965
Source noteuspto-grants-2013_07