HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109733Generated: October 30, 2026
HCID 20711242, compound → HCID 57634024, compound
https://huagongshe.com/reaction/2109733
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 20711242 | HCID 20711242 | — |
| Reactant | HCID 57633943 | HCID 57633943 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | HCID 57634024 | HCID 57634024 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514566B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-ceea7bd1cf7a448db36b19617a7da33b |
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| Source note | uspto-grants-2009_04 |
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