HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096987Generated: October 30, 2026
Triethylamine → N-(Cyclopropylmethyl)-2-(3-iodo-4-methylpyridin-2-yl)hydrazinecarboxamide
https://huagongshe.com/reaction/2096987
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclopropanemethanamine | HCID 75646 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | 2-Hydrazinyl-3-iodo-4-methylpyridine | HCID 58154301 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(Cyclopropylmethyl)-2-(3-iodo-4-methylpyridin-2-yl)hydrazinecarboxamide | HCID 66953986 | 188.9% |
Reaction Steps
A solution of cyclopropylmethanamine (0.33 mL, 3.7 mmol) in dichloromethane (2 mL) was added dropwise to a solution of triphosgene (0.39 g, 1.3 mmol) in dichloromethane (15 mL) kept at 0° C. under an argon atmosphere. After 5 minutes, a solution of triethylamine (1.0 mL, 7.2 mmol) in dichloromethane was added dropwise and the mixture was warmed to ambient tempertaure. After stirring two hours, the mixture was cooled to 0° C. and 2-hydrazinyl-3-iodo-4-methylpyridine (preparation 28b, 0.91 g, 3.6 mmol) in dichloromethane (8 mL) was added dropwise. The mixture was warmed to ambient temperature and stirred overnight. The solid precipitate was filtered, washed with diethyl ether and dried to yield the title compound (0.85 g, 68%) as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450341B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-59a3c3f022fd41d7b24663f0ee41860d |
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| Source note | uspto-grants-2013_05 |
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