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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077308Generated: November 3, 2026

Ammonium Chloride → HCID 66967852, compound

https://huagongshe.com/reaction/2077308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(2-trimethylsilanyl-ethoxymethyl)-1H-indoleHCID 11096925—
Reactanttert-Butyl 2-(methoxy(methyl)carbamoyl)piperidine-1-carboxylateHCID 21988510—
ReactantButyllithiumHCID 178418339—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 66967852HCID 6696785237%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

A stirring, ice-cooled solution of 1-(2-trimethylsilanyl-ethoxymethyl)-1H-indole, D66 (742 mg, 3 mmol) in DME (5 ml) was treated drop-wise with n-butyl lithium (2.2 ml, 1.6M in hexanes, 3.5 mmol). The resulting green solution was stirred at 0-5° C. for 15 min. then was treated with (RS)-1-(tert-butyloxycarbonyl)-2-(N-methoxy-N-methylcarbamoyl)-piperidine, D1 (952 mg, 3.5 mmol) in DME (2.5 ml). After stirring at this temperature for a further 45 min. saturated aqueous NH4Cl was added (10 ml) and the product was extracted with diethyl ether. The organics were combined, the solvent removed in vacuo and the residue chromatographed (silica gel, 10% diethyl ether-pentane) to afford the title compound as a colourless oil (510 mg, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928124B2
Source datasetuspto-grants-2011_04
ORD IDord-48f15c4fbca44d2f8c0805fd992491e9
Source noteuspto-grants-2011_04