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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515240Generated: October 31, 2026

Triethylamine → Tert-butyl 4-(3-{1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-2,2-dioxido-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridin-5-yl}-4-methylbenzyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/515240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant(3-{1-[(2,2-Difluorocyclopropyl)methyl]-3-methyl-2,2-dioxido-1,3 dihydro[1,2,5]thiadiazolo[3,4-b]pyridin-5-yl}-4-methylphenyl)methanolHCID 67409954—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductTert-butyl 4-(3-{1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-2,2-dioxido-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridin-5-yl}-4-methylbenzyl)piperazine-1-carboxylateHCID 67412149—

Reaction Conditions

Temperature80 °C

Reaction Steps

(3-{1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-2,2-dioxido-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridin-5-yl}-4-methylphenyl)methanol (39-1) (1.5 g, 3.8 mmol, 1.0 eq) was dissolved in NMP (19 mL) and triethylamine (1.6 mL, 11.4 mmol, 3.0 eq) was added followed by mesyl chloride (0.59 mL, 7.6 mmol, 2.0 eq). After 20 minutes, tert-butyl piperazine-1-carboxylate (1.8 g, 9.7 mmol, 3.0 eq) and DIPEA (2.8 mL, 16.2 mmol, 5.0 eq) were added. The resulting mixture stirred at 80° C. for 2 hours minutes. The mixture was cooled, diluted with EtOAc (200 mL), washed with sodium bicarbonate (50 mL), water (6×50 mL) and brine (50 mL), dried over MgSO4, filtered and concentrated. The crude residue was purified by flash chromatography (330 g SiO2, 0-80% EtOAc in hexanes) to afford tert-butyl 4-(3-{1-[(2,2-difluorocyclopropyl)methyl]-3-methyl-2,2-dioxido-1,3-dihydro[1,2,5]thiadiazolo[3,4-b]pyridin-5-yl}-4-methylbenzyl)piperazine-1-carboxylate (43-1) as a tan solid. HRMS m/z (M+H) 564.2446 found, 564.2451 required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108937B2
Source datasetuspto-grants-2015_08
ORD IDord-703c147c7d844dbf99e70771c6468aed
Source noteuspto-grants-2015_08