HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076017Generated: October 30, 2026
Diisopropylethylamine → HCID 44193964, compound
https://huagongshe.com/reaction/2076017
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67096250 | HCID 67096250 | — |
| Reactant | [3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]thiourea | HCID 71650841 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 44193964 | HCID 44193964 | 5.8% |
Reaction Steps
A suspension of [3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-thiourea (100 mg, 0.38 mmol) and of crude 6-bromo-2-(2-chloro-phenyl)-cyclohexanone hydrobromide (163 mg, 0.36 mmol) in ethanol (5 mL) was heated to reflux under an atmosphere of nitrogen for 2 days. N,N-diisopropyl ethyl amine (49 mg, 0.38 mmol) was added and the reaction was heated to reflux over night. After cooling to room temperature the solvent was evaporated under reduced pressure and the residue was treated with dichloromethane/methanol/concentrated aqueous NH4OH solution (9:1:0.1 v/v/v). The precipitate was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by reversed preparative HPLC using acetonitril/water (0.1% formic acid) to yield the title compound (6 mg, 3%) as a yellow solid. MS ISP (m/e): 541.9/543.9 (100/35) [(M+H)+]. 1H NMR (CDCl3, 300 MHz): δ (ppm)=7.60 (s, 1H), 7.37 (m, 2H), 7.26 (m, 5H), 7.09-7.18 (m, 4H), 6.82 (s, 1H), 6.66 (d, 1H), 4.70 (m, 1H), 3.74 (m, 3H), 3.60 (s, 3H), 3.19 (dd, 1H), 2.81 (dd, 1H), 2.28 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07923450B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-6f32f3fcc8c940b7aa20a6aa4934686d |
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| Source note | uspto-grants-2011_04 |
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