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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651702Generated: October 29, 2026

Ammonia → N-Methyl-3-(((2R)-1-methyl-2-pyrrolidinyl)methyl)-1H-indole-5-methanesulfonamide

https://huagongshe.com/reaction/651702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantAmmonium ChlorideHCID 25517—
ReactantCalciumHCID 5460341—
Reactant(R)-1-[1-benzyl-3-(1-methyl-2-pyrrolidinylmethyl)-1H-indol-5-yl]-N-diphenylmethyl-N-methylmethanesulfonamideHCID 57119402—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductN-Methyl-3-(((2R)-1-methyl-2-pyrrolidinyl)methyl)-1H-indole-5-methanesulfonamideHCID 13255273%

Reaction Steps

Into a stirred slurry of calcium tunings (1.11 g, 27.7 mmol) in tetrahydrofuran (1.2 ml) at −40° C. was added condensed liquid ammonia (16 ml). The blue bronze was stirred at −50 to −40° C. for a further 15 min, before a solution of (R)-1-[1-benzyl-3-(1-methyl-2-pyrrolidinylmethyl)-1H-indol-5-yl]-N-diphenylmethyl-N-methylmethanesulfonamide (from step (e), 4.0 g, 6.93 mmol) in tetrahydrofuran (10 ml) was added dropwise, maintaining the temperature below −40° C. The dark blue solution was stirred at −40° C. for a further 30 min, before saturated ammonium chloride solution (10 ml) was added dropwise and the grey solution warmed to ambient temperature. Water (10 ml) was then added and the white slurry stirred for 15 min, before being filtered in vacuo. The solid was then dissolved in 5N HCl (12 ml) and the resulting orange solution extracted with ethyl acetate (10 ml). The pH of the aqueous phase was then adjusted (pH=10) with 10N NaOH which resulted in precipitation. The solid was filtered and dried in vacuo at 50° C. overnight to yield the title compound (1.54 g, 73%) as a white solid. m.p. 209-212° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281357B1
Source datasetuspto-grants-2001_08
ORD IDord-0870a351c85144a7a1df8627e2a8a342
Source noteuspto-grants-2001_08