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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417487Generated: October 31, 2026

Water → HCID 54332622, compound

https://huagongshe.com/reaction/1417487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantMethanesulfonamideHCID 72879—
ReactantHCID 53645035HCID 53645035—
CatalystOxalyl chlorideHCID 65578—
SolventDichloromethaneHCID 6344—
ProductHCID 54332622HCID 5433262236.6%

Reaction Steps

0.055 ml (0.63 nmol) of oxalyl chloride was added, with ice-cooling, to a mixture of 100 mg (0.32 mmol) of (9-benzylcarbazol-2-yl)acetic acid (prepared as described in Example 42) in 3 ml of methylene chloride, and the whole was stirred for 30 minutes at room temperature. After this time, the solvent was removed by evaporation under reduced pressure. 5 ml of methylene chloride, 0.08 ml (0.99 mmol) of pyridine and 60 mg (0.63 mmol) of methanesulfonamide were added to the residue thus obtained, with ice-cooling. The reaction mixture was then stirred for 12 hours at room temperature. After the reaction had been allowed to go to completion, water was added to the reaction mixture, which was then extracted with ethyl acetate. The organic fraction was then washed with water and dried over anhydrous sodium sulfate, and the solvent was removed by evaporation under reduced pressure. The residue was purified by silica gel column chromatography, using 30 g of silica gel with a 50% v/v solution of methanol in ethyl acetate as eluent, to yield 46 mg of the title compound as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877199
Source datasetuspto-grants-1999_03
ORD IDord-a4264a63514e4b99acfd47476e8bab48
Source noteuspto-grants-1999_03