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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109733Generated: October 30, 2026

HCID 20711242, compound → HCID 57634024, compound

https://huagongshe.com/reaction/2109733

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 numberUS07514566B2
Source datasetuspto-grants-2009_04
ORD IDord-ceea7bd1cf7a448db36b19617a7da33b
Source noteuspto-grants-2009_04