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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504662Generated: October 26, 2026

Dimethylformamide → ethyl 7-amino-4-chloro-1-(methoxymethyl)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/504662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantChlorosuccinimideHCID 31398—
Reactantethyl 7-amino-1-(methoxymethyl)-1H-indole-2-carboxylateHCID 57475944—
SolventWaterHCID 962—
Productethyl 7-amino-4-chloro-1-(methoxymethyl)-1H-indole-2-carboxylateHCID 5747601825.1%

Reaction Steps

A mixture of ethyl 7-amino-1-(methoxymethyl)-1H-indole-2-carboxylate (3.18 g), N-chlorosuccinimide (1.74 g) and N,N-dimethylformamide (20 ml) was stirred overnight at room temperature. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The residue was subjected to silica gel column chromatography to give the title compound (0.91 g, yield 25%) as a yellow oil from a fraction eluted with ethyl acetate-hexane (1:4, volume ratio).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777047B2
Source datasetuspto-grants-2010_08
ORD IDord-7270b02e628f495d8139488d0960dc15
Source noteuspto-grants-2010_08