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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201816Generated: October 28, 2026

Trifluoroacetic acid → HCID 71061456, compound

https://huagongshe.com/reaction/2201816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 71061467HCID 71061467—
SolventDichloromethaneHCID 6344—
ProductHCID 71061456HCID 7106145695%

Reaction Steps

Trifluoroacetic acid (1.5 mL) was added drop wise to an ice-cooled suspension of benzyl 3-chloro-4-[(2,4,4-trimethylpentan-2-yl)amino]-1H-pyrrolo[3,2-c]pyridine-1-carboxylate (610 mg) in dichloromethane (10 mL). The reaction mixture was stirred at room temperature for about 4 hours. Upon completion, the reaction mixture was concentrated under vacuum and the residue was stirred in excess aqueous ammonia solution. The precipitated solid was filtered under suction, washed with water and dried to afford benzyl 4-amino-3-chloro-1H-pyrrolo[3,2-c]pyridine-1-carboxylate (354.8 mg, 95%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364466B2
Source datasetuspto-grants-2016_06
ORD IDord-af8ac1b4088540778346a1949436c12a
Source noteuspto-grants-2016_06