HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012227Generated: October 30, 2026
Hydrochloric Acid → 1-(6-Chloro-3-pyridylmethyl)-3-methyl2-nitroguanidine
https://huagongshe.com/reaction/1012227
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-(Aminomethyl)-2-chloropyridine | HCID 7020927 | — |
| Reactant | (E)-N-methyl-N'-nitromethoxymethanimidamide | HCID 136414659 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(6-Chloro-3-pyridylmethyl)-3-methyl2-nitroguanidine | HCID 136218196 | 88.9% |
Reaction Steps
1.3 g of sodium chloride and 4.65 g of water were mixed, and the resulting mixture was cooled to −10 degree centigrade. N,O-dimethyl-N′-nitroisourea (4.5 g, 0.03 mole) was introduced into the above solution, and 0.58 g (4.64 mmole) of 32% NaOH was further added to the suspension and stirred. Thereafter, [(2-chloro-5-pyridyl)methyl]amine (4.93 g, 0.03 mole) was introduced dropwise to the suspension. Sodium chloride was dissolved in water with 78% of the saturated solubility at a water temperature of −10 degree centigrade. The solution was stirred at −10 degree centigrade for 4 hours and then heated to 20 degree centigrade, and further stirred for 6 hours. Then, 35% hydrochloric acid (0.7 g, 6.71 mmole) was added to the suspension so that the pH became not more than 4. The resulting solution was extracted with ethyl acetate and concentrated under a reduced pressure, and then recrystallized. Thus, 6.5 g of a 1-[(2-chloro-5-pyridyl)methyl]-3-methyl-2-nitroguanidine was obtained. The isolated yield at this time was 81%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977496B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-92a3d774019c4b4781bba48825b47577 |
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| Source note | uspto-grants-2011_07 |
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