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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367048Generated: October 30, 2026

Water → HCID 23146402, compound

https://huagongshe.com/reaction/1367048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant2-Methyl-5-(4-fluorophenyl)thiazole-4-carbonyl chlorideHCID 22324119—
ReactantHCID 66967862HCID 66967862—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23146402HCID 23146402—
ProductHCID 66968449HCID 66968449—

Reaction Steps

(RS)-1-[5-(4-Fluoro-phenyl)-2-methyl-thiazol-4-yl]-1-{2-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-indol-2-ylmethyl]-piperidin-1-yl}-methanone (130 mg) was prepared from (RS)-2-piperidin-2-ylmethyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indole, D68 (520 mg) and 5-(4-fluoro-phenyl)-2-methyl-thiazole-4-carbonyl chloride (512 mg) according to a procedure similar to that for Example 1. A stirring solution of the above amide (125 mg) in dry THF (5 ml) was treated with a solution of tetrabutylammonium fluoride (2.2 mmol) in THF (5 ml). Once tlc indicated the reaction had gone to completion, the reaction mixture was poured into water and the product extracted with ethyl acetate. The combined organics were washed with brine, dried (Na2SO4) and the solvent removed in vacuo. Chromatography (silica gel, 0-100% pentane-ethyl acetate followed by preparative tlc, 40% ethyl acetate-pentane) afforded the title compound as a white solid (2.5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893090B2
Source datasetuspto-grants-2011_02
ORD IDord-7eadbd31c930415ea88fa77d98aa3877
Source noteuspto-grants-2011_02