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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011571Generated: October 30, 2026

Ammonia → 2-Aminocarbonylamino-5-(4-bromophenyl)pyrrole-3-carboxamide

https://huagongshe.com/reaction/1011571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
ReactantTrichloroacetyl isocyanateHCID 76400—
Reactant2-Amino-5-(4-bromophenyl)pyrrole-3-carboxamideHCID 59285978—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Aminocarbonylamino-5-(4-bromophenyl)pyrrole-3-carboxamideHCID 2500570436%

Reaction Steps

Trichloroacetyl isocyanate (60 μL, 0.50 mmol) was added dropwise to a solution of 2-amino-5-(4-bromophenyl)pyrrole-3-carboxamide (Reference compound No. 1-1, 0.17 g, 0.60 mmol) in anhydrous tetrahydrofuran (3.0 mL) at −40° C. and the mixture was stirred for 1 hour. Furthermore, ammonia solution 2.0 M in methanol (3.0 mL, 6.0 mmol) was added thereto, and the whole was stirred at room temperature for 3 days. Water (20 mL) was added to the reaction solution, then the precipitated solid was filtered off. The obtained solid was dried under reduced pressure to give the target compound (0.070 g) as a brown solid (Yield 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977371B2
Source datasetuspto-grants-2011_07
ORD IDord-1c7be30331e74cf3ab4d22d2ee4f973f
Source noteuspto-grants-2011_07