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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515238Generated: October 30, 2026

Diisobutylaluminum hydride → (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

https://huagongshe.com/reaction/515238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantMethyl 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-methylbenzoateHCID 67411535—
SolventTetrahydrofuranHCID 8028—
Product(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—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Methyl 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-methylbenzoate (38-1) (8.0 g, 18.9 mmol, 1.0 eq) dissolved in THF (100 mL) and cooled to −78° C. DIBAL-H (60.0 mL, 60.0 mmol, 3.2 eq, 1.0 M in heptane) was added and the mixture was stirred at the same temperature. After 10 minutes the reaction was carefully quenched by an addition of Rochelle's Salt (15 mL) and stirred for 3 hours warming to ambient temperature. The mixture was extracted with EtOAc (300 mL), washed with water (2×50 mL) and brine (50 mL), dried over MgSO4, filtered and concentrated to afford (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) as a tan solid. No further purification was necessary. HRMS m/z (M+H) 396.1188 found, 396.1188 required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108937B2
Source datasetuspto-grants-2015_08
ORD IDord-e57f77b6ccdf4dab82fe6e49ff2d22b4
Source noteuspto-grants-2015_08