HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345593Generated: October 26, 2026
Sodium Bicarbonate → cis-4-amino-5-chloro-2-methoxy-N-[3-methoxy-1-(2-pyrazinylmethyl)-4-piperidinyl]-benzamide
https://huagongshe.com/reaction/345593
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Amino-5-chloro-2-methoxy-N-[(3R,4S)-3-methoxypiperidin-4-YL]benzamide | HCID 9861621 | — |
| Reactant | Pyrazin-2-ylmethyl methanesulfonate | HCID 15096999 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | cis-4-amino-5-chloro-2-methoxy-N-[3-methoxy-1-(2-pyrazinylmethyl)-4-piperidinyl]-benzamide | HCID 15096934 | — |
Reaction Steps
4.7 Parts of cis-4-amino-5-chloro-2methoxy-N-(3-methoxy-4-piperidinyl)benzamide were dissolved in 160 parts of 2-propanone. Then there were added successively 3.2 parts of [(2-pyrazinyl)methyl] methanesulfonate (ester) and 1.7 parts of sodium hydrogen carbonate. The whole was stirred and refluxed for 18 hours while nitrogen gas was introduced. The precipitated product was filtered off and the filtrate was evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized twice from acetonitrile, yielding 1.16 parts of cis-4-amino-5-chloro-2-methoxy-N-[3-methoxy-1-(2-pyrazinylmethyl)-4-piperidinyl]-benzamide; mp. 203.5° C. (compound 144).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05057525 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-8a6dfbf548e44cfd9f83ea97e28ecc1f |
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| Source note | uspto-grants-1991_10 |
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