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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593284Generated: October 29, 2026

Cesium carbonate → HCID 68287864, compound

https://huagongshe.com/reaction/593284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant(4-Fluoro-2-methoxyphenyl)boronic acidHCID 2782672—
Reactant3-Amino-N-tert-butylbenzene-1-sulfonamideHCID 3162838—
Reactant2-Fluoro-4-iodopyridineHCID 7023570—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 68287864HCID 682878645%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 2-fluoro-4-iodopyridine (100 mg, 0.45 mmol), 3-amino-N-(tert-butyl)benzenesulfonamide (153 mg, 0.67 mmol), and Cs2CO3 (291 mg, 0.89 mmol) in dry DMF (3 mL) was heated at 150° C. for 1.5 h in a microwave oven. After addition of (4-fluoro-2-methoxyphenyl)boronic acid (152 mg, 0.89 mmol) the mixture was degassed with a stream of nitrogen for 5 minutes. Pd(dppf)Cl2 (73 mg, 0.09 mmol) was added and the reaction mixture was heated to 140° C. for 90 minutes in a microwave oven. The mixture was diluted with EtOAc and washed twice with sat. aq. NaHCO3-solution and once with brine. The organic layer was dried over MgSO4 and concentrated under reduced pressure, and the residue was purified by preparative HPLC (water/ACN 95:5 to 0:100) to yield the desired product D2 as a yellow solid (9 mg, 5%). 1H NMR (400 MHz, d6-DMSO, 300K) δ 1.12 (s, 9H), 3.82 (s, 3H), 6.89 (m, 2H), 6.97 (s, 1H), 7.06 (dd, J=11.5 Hz, J=2.4 Hz, 1H), 7.30 (d, J=8.0 Hz, 1H), 7.39 (m, 2H), 7.44 (s, 1H), 7.87 (d, J=8.0 Hz, 1H), 8.18 (d, J=5.4 Hz, 1H), 8.24 (m, 1H), 9.39 (s, 1H). MS (ES) C22H24FN3O3S requires: 429. found: 430 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242937B2
Source datasetuspto-grants-2016_01
ORD IDord-c55b9e75be5e4f4da25ab333fd8ca1a5
Source noteuspto-grants-2016_01