HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246782Generated: November 1, 2026
Ammonia → 1-(6-Chloro-3-pyridinyl)cyclopropanecarboxamide
https://huagongshe.com/reaction/2246782
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 1-(6-Chloropyridin-3-yl)cyclopropane-1-carboxylic acid | HCID 59216308 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-(6-Chloro-3-pyridinyl)cyclopropanecarboxamide | HCID 71743267 | — |
Reaction Steps
To a 0° C. solution of 1-(6-chloropyridin-3-yl)cyclopropanecarboxylic from Step 4 (1.0 g) in chloroform (50 mL) were slowly added isobutyl chloroformate (800 μL) and triethylamine (920 μL). The reaction mixture was stirred at 0° C. for 2 hours. Then it was saturated with ammonia gas and stirred at 0° C. for 10 minutes. The reaction mixture was allowed to stand at room temperature for 1 hour then poured into water (80 mL) and partitioned. The aqueous layer was extracted with dichloromethane (2×80 mL). The combined extracts were washed with brine, dried with magnesium sulfate and the solvent removed in vacuo. The residue was purified by swish using diethyl ether and hexanes to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687524B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-d2390e9d5fcb4aec8f8717a51dfac4ca |
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| Source note | uspto-grants-2010_03 |
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