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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457682Generated: October 26, 2026

Carbonyl bromide → N-[4-(Isopropylformylamino)cyclohexyl]methylthiourea

https://huagongshe.com/reaction/457682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbonyl bromideHCID 79057—
ReactantDiisopropylethylamineHCID 81531—
ReactantThioureaHCID 2723790—
ReactantHCID 17946834HCID 17946834—
SolventEthanolHCID 702—
ProductN-[4-(Isopropylformylamino)cyclohexyl]methylthioureaHCID 22254060—

Reaction Steps

A thiourea such as N-[4-(isopropylformylamino)cyclohexyl]-methylthiourea (0.029 mmol, 1 equivalent), a bromoketone (0.044 mmol, 1.5 equivalent) and 2 equivalents of diisopropylethyl amine in 10 ml of EtOH were heated at reflux temperature for 2 days. The reaction mixture was concentrated in vacuo and the crude product chromatographed (silica) to obtain the desired product. This procedure was used to prepare examples 101–102.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189720B2
Source datasetuspto-grants-2007_03
ORD IDord-ee9773061a0943b58a1861525ed730a9
Source noteuspto-grants-2007_03