HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906315Generated: October 31, 2026
Hydrochloric Acid → N-[5-(benzyloxy)pyrimidin-2-yl]hexanamide
https://huagongshe.com/reaction/906315
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hexanoyl chloride | HCID 67340 | — |
| Reactant | 5-(Benzyloxy)pyrimidin-2-amine | HCID 20748397 | — |
| Catalyst | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[5-(benzyloxy)pyrimidin-2-yl]hexanamide | HCID 67391208 | 96,982.203% |
Reaction Steps
A solution of 5-(benzyloxy)pyrimidin-2-amine (60.0 g, 0.30 mmol) in dichloromethane (400 mL) was added with pyridine (30 mL, 0.37 mmol), the mixture was added dropwise with a solution of hexanoyl chloride (46 g, 0.34 mmol) in dichloromethane (100 mL) with stirring on an ice bath, and the mixture was stirred at the same temperature for 1 hour. The reaction mixture was added with 1 M hydrochloric acid (500 mL), and extracted with chloroform, and the organic layer was successively washed with water and saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was recrystallized froth chloroform-hexane to obtain N-[5-(benzyloxy)pyrimidin-2-yl]hexanamide (87.1 g, 98%) as colorless acicular crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012989B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-47b5bde350c84af7908ca237e55315e5 |
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| Source note | uspto-grants-2011_09 |
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