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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741565Generated: October 30, 2026

Methanol → Quinolizidin-2-ylmethyl-2-methoxyindole-3-carboxylate

https://huagongshe.com/reaction/741565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantChlorosuccinimideHCID 31398—
ReactantQuinolizidin-2-ylmethylindole-3-carboxylateHCID 131719520—
SolventChloroformHCID 6212—
ProductQuinolizidin-2-ylmethyl-2-methoxyindole-3-carboxylateHCID 131719529—

Reaction Steps

A stirred solution of N-chlorosuccinimide (220 mg, 0.0016 mole) in chloroform (6 ml) at room temperature under nitrogen was treated with a solution of eq-quinolizidin-2-ylmethylindole-3-carboxylate (E9b) (330 mg, 0.0011 mole) in chloroform (6 ml) and stirred for 2 h. The solution was then treated with methanol (0.71 ml, 0.022 mole) and stirring continued. After 3 h a beige precipitate began to form and afar a further 1 h this was filtered off, washed with chloroform,and dried to afford the title compound (E26) as its hydrochloride salt mp 212°-213° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552398
Source datasetuspto-grants-1996_09
ORD IDord-1279c910acfc474caf79b15ed317f30c
Source noteuspto-grants-1996_09