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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522698Generated: October 25, 2026

1H-Imidazole-1-propanamine → 2-Bromo-N-[3-(1H-imidazol-1-yl)propyl]-5-thiazolecarboxamide

https://huagongshe.com/reaction/522698

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Imidazole-1-propanamineHCID 78736—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant2-Bromothiazole-5-carboxylic acidHCID 2763210—
SolventDichloromethaneHCID 6344—
Product2-Bromo-N-[3-(1H-imidazol-1-yl)propyl]-5-thiazolecarboxamideHCID 90013374—

Reaction Conditions

Temperature25 °C

Reaction Steps

2-Bromothiazole-5-carboxylic acid (0.4 g, 1.923 mmol), 3-(1H-imidazole-1-yl)propan-1-amine (0.265 g, 2.115 mmol), and benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (BOP) (0.935 g, 2.115 mmol) were mixed in dichloromethane (7 ml), treated with Hunig's base (0.705 ml, 4.04 mmol) and stirred at 25° C. for 2 hours. The reaction mixture was diluted with dichloromethane and washed with water and brine. The organic layer was dried (MgSO4), filtered and concentrated. Purification by flash chromatography (silica gel, 2-20% methanol/dichloromethane) afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334264B2
Source datasetuspto-grants-2016_05
ORD IDord-a99bcaaa48f845cf97ba0762728366ac
Source noteuspto-grants-2016_05