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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201692Generated: October 26, 2026

Isopropyl isocyanate → Tert-butyl (2-(3-isopropylureido)-4-(thiophen-2-yl)phenyl)carbamate

https://huagongshe.com/reaction/2201692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl isocyanateHCID 61277—
Reactanttert-Butyl (2-amino-4-(thiophen-2-yl)phenyl)carbamateHCID 57717474—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductTert-butyl (2-(3-isopropylureido)-4-(thiophen-2-yl)phenyl)carbamateHCID 7100731670%

Reaction Steps

To a solution of tert-butyl (2-amino-4-(thiophen-2-yl)phenyl)carbamate (0.20 g, 0.70 mmol, 1.0 equiv.) in dichloromethane (4 mL) was added isopropyl isocyanate (0.07 mL, 0.83 mmol, 1.2 equiv.) and TEA (0.19 mL, 1.37 mmol) at 0° C. The reaction was stirred at room temperature for 16 h. The reaction was then diluted with dichloromethane and water. The organic layer was separated, washed with water and brine, dried over sodium sulfate, then concentrated under reduced pressure. The crude material was purified by column chromatography (silica gel, 20% EtOAc/hexanes) to give tert-butyl (2-(3-isopropylureido)-4-(thiophen-2-yl)phenyl)carbamate (0.18 g, 70% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365498B2
Source datasetuspto-grants-2016_06
ORD IDord-dc781329b270497d9f1b40b46dde256e
Source noteuspto-grants-2016_06