HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69423Generated: October 26, 2026
Hydrochloric Acid → 6-Butoxy-2-[4-(3-dimethylaminopyrrolidin-1-yl)-3-fluorophenyl]-2H-isoquinolin-1-one
https://huagongshe.com/reaction/69423
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 4-butoxy-N-[4-(3-dimethylaminopyrrolidin-1-yl)-3-fluorophenyl]-2-methylbenzamide | HCID 68990568 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Butoxy-2-[4-(3-dimethylaminopyrrolidin-1-yl)-3-fluorophenyl]-2H-isoquinolin-1-one | HCID 57916768 | — |
Reaction Steps
n-Butyllithium (2.6M in toluene; 0.70 mL) was added to a solution of N,N-diisopropylamine (184 mg) in THF (30 mL) at −78° C. After 10 minutes, 4-butoxy-N-[4-(3-dimethylaminopyrrolidin-1-yl)-3-fluorophenyl]-2-methylbenzamide (0.30 g) was added, and the mixture was stirred at −78° C. for 30 minutes and then warmed to −20° C. DMF (53 mg) was added, and the reaction mixture was hydrolyzed after a further 30 minutes with hydrochloric acid. The reaction mixture was partitioned between sodium carbonate solution and ethyl acetate. The organic phase was dried over sodium sulfate and concentrated. The residue was purified by preparative HPLC. The product with the molecular weight of 423.54 (C25H30FN3O2) was obtained in this way; MS (ESI): 424 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822495B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-8ba8bc138ec249ef952b5f6c4cd4fac5 |
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| Source note | uspto-grants-2014_09 |
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