HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439906Generated: October 25, 2026
Ammonia → 4-(2-(5-Methylpyrazine-2-carboxamido)ethyl)benzenesulfonamide
https://huagongshe.com/reaction/439906
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | N-[2-[4-chlorosulfonylphenyl]ethyl]-5-methylpyrazine carboxamide | HCID 22409115 | — |
| Product | 4-(2-(5-Methylpyrazine-2-carboxamido)ethyl)benzenesulfonamide | HCID 9883549 | — |
Reaction Steps
According to the invention there is provided a process for the preparation of N-[2-[4-(aminosulfonyl)phenyl]ethyl]-5-methylpyrazine-carboxamide of the formula I: ##STR15## consisting of: i) treating 5-methylpyrazine-2-carboxylic acid of the formula VIII: ##STR16## with methanol under reflux to obtain 5-methylpyrazine-2-carboxylic acid methyl ester of the formula VIII A ##STR17## ii) reacting 5-methylpyrazine-2-carboxylic acid methyl ester of the formula VIII A with 2-phenylethylamine of the formula II: ##STR18## at 100° to 200° C. to obtain 5-methylpyrazine 2-(2-phenylethyl) carboxamide of the formula IX: ##STR19## iii) chlorosulfonating the 5-methylpyrazine-2(2-phenylethyl)carboxamide of the formula IX with chlorosulfonic acid at 0°-45° C. to obtain [N-[2-[4-Chlorosulfonyl)phenyl]ethyl]-5-methylpyrazine carboxamide] of the formula X: ##STR20## iv) and treating the (N-[2-[4-(chlorosulfonyl)phenyl]ethyl]-5-methyl pyrazine-carboxamide] of the formula X with ammonia to obtain N-[2-[4-(aminosulfonyl)phenyl]ethyl]-5-methylpyrazine carboxamide of the formula I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05516906 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-56eccb1263074b76be970c22a7b7f1ea |
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| Source note | uspto-grants-1996_05 |
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