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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924144Generated: November 1, 2026

Diisopropylethylamine → N-(4-(chlorodifluoromethoxy)phenyl)-6-((3R,4R)-3,4-dihydroxypyrrolidin-1-yl)-5-iodonicotinamide

https://huagongshe.com/reaction/924144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(3R,4R)-pyrrolidine-3,4-diolHCID 11499204—
Reactant6-chloro-N-(4-(chlorodifluoromethoxy)phenyl)-5-iodonicotinamideHCID 86702626—
SolventIsopropanolHCID 3776—
ProductN-(4-(chlorodifluoromethoxy)phenyl)-6-((3R,4R)-3,4-dihydroxypyrrolidin-1-yl)-5-iodonicotinamideHCID 89906772—

Reaction Conditions

Temperature140 °C

Reaction Steps

To a solution of 6-chloro-N-(4-(chlorodifluoromethoxy)phenyl)-5-iodonicotinamide (Stage 247.2, 300 mg, 0.654 mmol) and (3R,4R)-pyrrolidine-3,4-diol (88 mg, 0.850 mmol) in iPrOH (5 mL) was added DIPEA (0.228 mL, 1.307 mmol). The RM was stirred at 140° C. for 1 h and then 3 h at 130° C. The solvent was evaporated off under reduced pressure to give the crude product which was used directly without any further purification. UPLC-MS (Condition 3), tR=1.00 min, m/z=525.9/528.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278981B2
Source datasetuspto-grants-2016_03
ORD IDord-0b21ba1462f54fb2ae81f785c3048355
Source noteuspto-grants-2016_03