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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023733Generated: October 30, 2026

Ethyl 5-Bromoindole-2-carboxylate → HCID 67395583, compound

https://huagongshe.com/reaction/1023733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-Bromoindole-2-carboxylateHCID 259091—
ReactantHCID 58420521HCID 58420521—
ProductHCID 67395583HCID 6739558332.3%

Reaction Steps

In the same manner as that of Example 32, 4,5-diisopropylfuran-2-carboxamide (71 mg, 0.364 mmol) and ethyl 5-bromoindole-2-carboxylate (195 mg, 0.728 mmol) were coupled. The reaction mixture was treated in a conventional manner, and the resultant was purified by silica gel chromatography [hexane-ethyl acetate (4:1), and 1% methanol-chloroform] and then recrystallized to obtain ethyl 5-[(4,5-diisopropylfuran-2-carbonyl)amino]-2-indolecarboxylate (45 mg, 32%) as colorless prisms, together with the collected starting material (39 mg, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722730B2
Source datasetuspto-grants-2014_05
ORD IDord-5442dc53d52e4c04a8adfa24f16fd73a
Source noteuspto-grants-2014_05