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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450122Generated: October 30, 2026

Boron tribromide → 5-Chloro-7-(2-fluoro-4-iodo-phenylamino)-pyrrolo[1,2-c]pyrimidine-6-carboxylic acid

https://huagongshe.com/reaction/450122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant5-Chloro-7-(2-fluoro-4-iodo-phenylamino)-pyrrolo[1,2-c]pyrimidine-6-carboxylic acid methyl esterHCID 67234910—
SolventDichloromethaneHCID 6344—
Product5-Chloro-7-(2-fluoro-4-iodo-phenylamino)-pyrrolo[1,2-c]pyrimidine-6-carboxylic acidHCID 67234860115.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-chloro-7-(2-fluoro-4-iodo-phenylamino)-pyrrolo[1,2-c]pyrimidine-6-carboxylic acid methyl ester (300 mg, 0.67 mmol) in DCM (6 mL) was added boron tribromide (0.65 mL, 6.7 mmol). The reaction was heated at reflux for 1 hour. The reaction mixture was cooled to 0° C. and carefully quenched by the addition of water (5 mL). The reaction mixture was diluted with aqueous hydrochloric acid (2 mL, 1M) and extracted with ethyl acetate (3×10 mL). The combined organic fractions were washed with brine, dried (MgSO4) and concentrated in vacuo to give the product as a dark brown solid (335 mg, 115%). LCMS (Method B): RT=3.58 min, M+H+=432.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486963B2
Source datasetuspto-grants-2013_07
ORD IDord-c8edf95a09bb46c4a41384c89b85ce1a
Source noteuspto-grants-2013_07