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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854935Generated: October 30, 2026

ethyl 6-chloro-8-iodo-2-(trifluoromethyl)-2H-chromene-3-carboxylate → ethyl 8-{[4-(aminosulfonyl)phenyl]ethynyl}-6-chloro-2-(trifluoromethyl)-2H-chromene-3-carboxylate

https://huagongshe.com/reaction/854935

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 6-chloro-8-iodo-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 21883552—
Reactant4-EthynylbenzenesulfonamideHCID 44457221—
Productethyl 8-{[4-(aminosulfonyl)phenyl]ethynyl}-6-chloro-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 69516710—

Reaction Steps

Ethyl 6-chloro-8-iodo-2-(trifluoromethyl)-2H-chromene-3-carboxylate prepared as in U.S. Pat. No. 6,271,253 B1 Example 73, Step 2 was reacted with 4-ethynylbenzene sulfonamide prepared as in Step 2 via a method similar to that described in Example 21f, Step 1 to give the product: ESHRMS m/z 503.0686 (M+NH4, C21H15ClF3O5SNH4, Calc'd 503.0655).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-bd33477bd92943ad98b00dc2e1d2d4ee
Source noteuspto-grants-2007_08