HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096484Generated: October 31, 2026
[2-(Dimethylcarbamoyl)phenyl]boronic acid → HCID 58423810, compound
https://huagongshe.com/reaction/2096484
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | [2-(Dimethylcarbamoyl)phenyl]boronic acid | HCID 44119823 | — |
| Reactant | 2'-amino-6-bromo-1'-methyl-2-phenylspiro[chroman-4,4'-imidazol]-5'(1'H)-one | HCID 58423768 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Cesium carbonate | HCID 10796 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 58423810 | HCID 58423810 | 6.8% |
Reaction Steps
Pd(PPh3)2Cl2 (10 mg, 0.01 mmol) in a 10 mL flask under Ar was treated sequentially with 2′-amino-6-bromo-1′-methyl-2-phenylspiro[chroman-4,4′-imidazol]-5′(1′H)-one (20 mg, 0.052 mmol) in 1,4-dioxane (1 mL), Cs2CO3 (2 N, 0.3 mL) and 2-(dimethylcarbamoyl)phenylboronic acid (20 mg, 0.104 mmol). The mixture was heated at 120° C. under Ar in a microwave reactor for 30 minutes. The reaction mixture was concentrated in vacuo to give the residue, which was purified by preparative TLC to give 2-(2′-amino-1′-methyl-5′-oxo-2-phenyl-1′,5′-dihydrospiro[chroman-4,4′-imidazole]-6-yl)-N,N-dimethylbenzamide (1.60 mg, 6%). 1H-NMR (MeOD): 2.45 (m, 3H), 2.56 (m, 1H), 2.64 (m, 1H), 2.86 (m, 3H), 3.36 (s, 3H), 5.81 (m, 1H), 7.14 (m, 1H), 7.21 (m, 1H), 7.33 (m, 1H), 7.44 (m,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450308B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-c586206a28f94d78a21f3a36c7f35d35 |
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| Source note | uspto-grants-2013_05 |
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