HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610500Generated: October 31, 2026
Benzoyl chloride → HCID 11067619, compound
https://huagongshe.com/reaction/610500
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 3-(1-Methyl-piperidin-4-yl)-1H-pyrrolo[3,2-b]pyridin-5-ylamine | HCID 10220230 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11067619 | HCID 11067619 | 66.1% |
Reaction Steps
To a solution of 0.100 gm (0.43 mMol) 5-amino-3-(1-methylpiperidin-4-yl)pyrrolo[3,2-b]pyridine in 3 mL 50% aqueous tetrahydrofuran were added 0.43 mL (0.86 mMol) benzoyl chloride and the resulting mixture was stirred at room temperature. After about 4 hours the reaction mixture was partitioned between dichloromethane and 2N sodium hydroxide. The phases were separated and the aqueous phase extracted well with dichloromethane. The organic phases were combined, dried over sodium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with a gradient of dichloromethane (2-10% methanol) containing 1% ammonium hydroxide. Fractions containing product were combined and concentrated under reduced pressure to provide 0.095 gm (66%) of the title compound. A portion was recrystallized from ethanol/water to provide an analytical sample.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998622 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-741f7bb5013940d487b01bfb245f8afa |
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| Source note | uspto-grants-1999_12 |
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