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CAS No. : | 26116-12-1 | MDL No. : | MFCD00003178 |
Formula : | C7H16N2 | Boiling Point : | - |
Linear Structure Formula : | H2NCH2(C4NH7)C2H5 | InChI Key : | UNRBEYYLYRXYCG-UHFFFAOYSA-N |
M.W : | 128.22 | Pubchem ID : | 117295 |
Synonyms : |
|
Chemical Name : | 2-(Aminomethyl)-1-ethylpyrrolidine |
Signal Word: | Danger | Class: | 3,8 |
Precautionary Statements: | P280-P305+P351+P338-P310 | UN#: | 2733 |
Hazard Statements: | H225-H314 | Packing Group: | Ⅲ |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
61% | With triethylamine; In water; acetone; | N-(1-ethyl 2-pyrrolidylmethyl) 2-methoxy 4-amino 5-ethylsulphonyl benzamide 81 g of <strong>[71675-87-1]2-methoxy 4-amino 5-ethylsulphonyl benzoic acid</strong> and 297 cm3 of acetone are placed in a flask fitted with an agitator, a thermometer and a dropping funnel, followed by 33 g of triethylamine. The solution is cooled to 0° C., then 30 g of ethyl chloroformate is added drop by drop between 0° and 5° C. When the mixture has been agitated 51 g of 1-ethyl 2-amino methyl pyrrolidine is added drop by drop between 5° and 10° C. The mixture is agitated at 10° C. then at ambient temperature. The triethylamine hydrochloride which precipitates is drained, then the acetone is distilled. The residue is dissolved in 600 cm3 of water in the presence of caustic soda solution. The base crystallises after seeding and is drained, washed with water and dried. When the crystals have been purified by passing them through hydrochloride and re-crystallising them in acetone, 66 g of N-[1-ethyl 2-pyrrolidylmethyl] 2-methoxy 4-amino 5-ethylsulphonyl benzamide is obtained (yield 61percent-M.P.=126° to 127° C.). |
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