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CAS No. : | 207557-35-5 | MDL No. : | MFCD08689902 |
Formula : | C7H9ClN2O | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | YCWRPKBYQZOLCD-LURJTMIESA-N |
M.W : | 172.61 | Pubchem ID : | 11073883 |
Synonyms : |
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Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P501-P261-P270-P271-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330-P304+P340+P312-P403+P233-P405 | UN#: | N/A |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
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* 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 |
---|---|---|
Example 97 (2S)-1-[1,1-Dimethyl-3-(3-pyridin-3-yl-pyrazol-1-yl)-propylamino]-acetyl}-pyrrolidine-2-carbonitrile, Methanesulfonic Acid Salt This compound was made in analogy to example 78, steps C] to D] from 3-(1H-pyrazol-3-yl)-pyridine (synthesised according to the literature: Plate et al., Bioorg. Med. Chem. 1996, 4 (2), 227 and Schunack, Arch. Pharm. 1973, 306, 934, 941), 4,4-dimethyl-2,2-dioxo-2λ'-[1,2,3]oxathiazinane-3-carboxylic acid tert-butyl ester and IIA as a methanesulfonic acid addition salt. MS (ISP): 367.3 (MH+, free base). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Example 112 (2S)-1-[(1S)-1-Methyl-2-(5-methyl-3-phenyl-pyrazol-1-yl)-ethylamino]-acetyl}-pyrrolidine-2-carbonitrile The title compound was obtained in analogy to example 78, steps C] to E] from <strong>[3347-62-4]5-methyl-3-phenyl-1H-pyrazole</strong> by replacing sulfimidate XIX with IV and with the exception, that the final coupling step with IIA was done as described in example 1. The title compound was obtained as the free amine as a glass. MS (ISP): 352.4 (MH+). |
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