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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951642Generated: October 26, 2026

Lithium Hydroxide → HCID 44818729, compound

https://huagongshe.com/reaction/1951642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactant4-MethylmorpholineHCID 7972—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantMethyl 4-((1S)-1-aminoethyl)benzoateHCID 17751895—
Reactant2-Methyl-4-(4-(trifluoromethyl)benzyl)-4H-thieno[3,2-b]pyrrole-3-carboxylic acidHCID 67182624—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 44818729HCID 4481872947%

Reaction Steps

A mixture of 0.043 g of 2-methyl-4-(4-trifluoromethyl-benzyl)-4H-thieno[3,2-b]pyrrole-3-carboxylic acid, 0.060 g of (S)-4-(1-amino-ethyl)-benzoic acid methyl ester, 0.040 g of HOBT-hydrate, 0.054 g of ethyl-dimethylaminopropyl-carbodiimide hydrochloride (EDCI) and 0.060 ml of N-methylmorpholine in 2 ml of DMF was stirred at room temperature for 18 h. The reaction was then quenched with 1 ml of water and 2 ml of saturated NaHCO3 solution. The resulting mixture extracted with 15 ml of EtOAc. The organic layer was dried over Na2SO4, filtered, and concentrated to give the crude methyl ester which was dissolved in 2 ml THF, 2 mL MeOH and 0.5 mL water and treated with 0.5 mL of 1M LiOH solution. After stirring for 24 h at room temperature, the reaction mixture was concentrated under reduced pressure to remove THF and MeOH. The residue was diluted with 2 mL of water and treated with 0.3 mL of AcOH with vigorous stirring. After stirring for 2 h, the solid was collected by filtration and air-dried to give 0.029 g of the title compound as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404736B2
Source datasetuspto-grants-2013_03
ORD IDord-d4a17d1c805a4cbfa9afabf65f2dc547
Source noteuspto-grants-2013_03