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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14169Generated: October 26, 2026

Methanesulfonyl chloride → Methyl 4-[(methylsulfonyl)amino]-1H-indole-6-carboxylate

https://huagongshe.com/reaction/14169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantMethyl 4-amino-1H-indole-6-carboxylateHCID 14243967—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-[(methylsulfonyl)amino]-1H-indole-6-carboxylateHCID 2108620850.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of methyl 4-amino-1H-indole-6-carboxylate (1.0 g) in DMF (10 mL) was added 4-dimethylaminopyridine (1.46 g) and methanesulfonyl chloride (0.6 g). The mixture was heated to 60° C. for 3 h, cooled to room temperature, and partitioned between water and ethyl acetate. The layers were separated and the organic layer washed three times with brine, dried over anhydrous sodium sulfate and concentrated to give 0.71 g of the title compound: 1H NMR (CDCl3) δ 3.02, 3.94, 6.69, 7.42, 7.81, 8.04.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727997B2
Source datasetuspto-grants-2010_06
ORD IDord-af7cd9f759014a5f8832d2a50b3f6f11
Source noteuspto-grants-2010_06