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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661060Generated: November 2, 2026

HCID 20711242, compound → HCID 57634024, compound

https://huagongshe.com/reaction/661060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20711242HCID 20711242—
ReactantHCID 57633943HCID 57633943—
SolventEthanolHCID 702—
SolventDiisopropylethylamineHCID 81531—
ProductHCID 57634024HCID 57634024—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of (S)-tert-butyl 3-(4-chlorophenyl)-1-thioureidopropan-2-ylcarbamate (0.585 g, 1.70 mmol) and ethyl 2-bromo-2-(3,4-difluorophenyl)acetate (0.500 g, 1.79 mmol) in ethyl alcohol (2 mL) and diisopropylethylamine (0.3 mL) in a sealed vial (Biotage microwave vial, 5 mL) with a magnetic stirring bar was heated in a microwave oven (Initiator, Biotage) at 120° C. for 15 minutes. After cooling to ambient temperature, the volatiles were removed in vacuum. The residue was partitioned between EtOAc and water. The combined organic portions were washed with brine. The crude product was purified by flash column chromatography (20% of EtOAc in hexanes for 5 minutes, 20% to 100% of EtOAc in hexanes over 23 minutes). The product was obtained as a white solid, 0.201 g, 24%. 1H NMR (300 MHz, CD3OD) δ 1.22-1.39 (m, 9H), 2.52-2.97 (m, 2H), 3.35-3.60 (m, 1H), 3.64-3.85 (m, 1H), 3.92-4.24 (m, 1H), 7.11-7.46 (m, 7H). LCMS (API-ES): 496.1/498.1 (M++H), chloro pattern.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084479B2
Source datasetuspto-grants-2011_12
ORD IDord-2ea9a9d97c604704aa614a56a6dec230
Source noteuspto-grants-2011_12