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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239533Generated: November 1, 2026

HCID 57989824, compound → HCID 57989626, compound

https://huagongshe.com/reaction/239533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57989824HCID 57989824—
SolventDichloromethaneHCID 6344—
ProductHCID 57989626HCID 5798962673.4%

Reaction Steps

To a suspension of N-{3-[5-(2-cyano-4-pyrimidinyl)-2-(4-morpholinyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2,5-difluorobenzenesulfonamide (2.12 g, 3.80 mmol) in dichloromethane (DCM) (38.0 ml) at −78° C. was added DI BAL-H (18.98 ml, 18.98 mmol). The yellow suspension was slowly warmed to RT and stirred 1 hr. The reaction was quenched with Rochelle's salts and stirred about 1 hr. 4N HCl was added to clear the emulsion. The HCl solution was extracted with DCM (3×). The aqueous was passed through celite and neutralize with 6N NaOH. Solid formed during neutralizing and was filtered to obtain N-{3-[5-[2-(aminomethyl)-4-pyrimidinyl]-2-(4-morpholinyl)-1,3-thiazol-4-yl]-2-fluorophenyl}-2,5-difluorobenzenesulfonamide (1.57 g, 73%). MS (ESI): 563 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642759B2
Source datasetuspto-grants-2014_02
ORD IDord-4ef235b208d84a77bf3315f69d37a1d1
Source noteuspto-grants-2014_02