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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372893Generated: October 30, 2026

Sodium Hydroxide → HCID 21072794, compound

https://huagongshe.com/reaction/1372893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantRed-AlHCID 16684438—
Reactant(4-(4-Fluoro-2-methyl-phenyl)-6-thiomorpholin-4-yl-pyridin-3-yl]-carbamic acid methyl esterHCID 21072793—
SolventTolueneHCID 1140—
ProductHCID 21072794HCID 21072794103%

Reaction Conditions

Temperature50 °C

Reaction Steps

43.7 ml Red-Al (3.5 M in toluene) was diluted in 25 ml toluene and added dropwise to a solution of 13 g (30.6 mmol) [4-(4-fluoro-2-methyl-phenyl)-6-thiomorpholin-4-yl-pyridin-3-yl]-carbamic acid methyl ester in 55 ml toluene at 10° C. (the addition was exothermic). The yellow solution obtained was stirred for 40 minutes at room temperature and 1.5 hours at 50° C. It was cooled to 0° C. and poured slowly onto a mixture of 150 ml 4 N aqueous sodium hydroxide and 50 ml ice (very exothermic). After 10 minutes stirring, the phases were separated, the aqueous phase was extracted with tert-butyl-methyl-ether and the organic phases were washed with brine. The combined organic extracts were dried and concentrated under reduced pressure to yield 10 g methyl-[4-(4-fluoro-2-methyl-phenyl)-6-thiomorpholin-4-yl-pyridin-3-yl]-amine as a brown oil which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160881B2
Source datasetuspto-grants-2007_01
ORD IDord-0f1e6ebcf02047a28d92e4c758403db7
Source noteuspto-grants-2007_01