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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766159Generated: November 2, 2026

Oxalyl chloride → HCID 86760497, compound

https://huagongshe.com/reaction/1766159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 21110052HCID 21110052—
SolventDichloromethaneHCID 6344—
ProductHCID 86760497HCID 86760497—

Reaction Conditions

Temperature20 °C

Reaction Steps

0.52 cm3 (6 mmol) of oxalyl chloride was added, under an argon atmosphere, to 1-(4-(methylsulfonyl)phenyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid in 15 cm3 of dichloromethane. After stirring at a temperature in the region of 20° C. for 300 h, the reaction mixture was concentrated to dryness under reduced pressure (2.7 kPa). The residue was triturated with 20 cm3 of dichloromethane, filtered and pulled dry, and then the solid was washed with 50 cm3 of distilled water to give, after drying, 0.13 g of bis[1-(4-(methylsulfonyl)phenyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic]anhydride in the form of a powder which was used directly in the following stage. IR spectrum (KBr): 3116, 2926, 1767, 1705, 1592, 1537, 1421, 1294, 1177, 1151, 1083, 999, 962, 775, 551 and 532 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230007B2
Source datasetuspto-grants-2007_06
ORD IDord-b91a090887c2445080afc1d545e793ee
Source noteuspto-grants-2007_06