HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446671Generated: October 31, 2026
Hydrochloric Acid → HCID 57448670, compound
https://huagongshe.com/reaction/446671
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 16045463 | HCID 16045463 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57448670 | HCID 57448670 | 25% |
Reaction Steps
To a stirred solution of 3-cyano-N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)benzenesulfonamide (0.20 g, 0.44 mmol), prepared using procedures similar to those described in Example 115, in dimethylformamide (1.2 mL) at 50° C. were added sodium azide (0.11 g, 1.76 mmol) and ammonium chloride (94 mg, 1.76 mmol). The crude mixture was heated at 100° C. overnight. The reaction was cooled to room temperature treated with ice water (20 mL) followed by concentrated hydrochloric acid (10 mL). The solid obtained was filtered under reduced pressure and washed with hexane (20 mL), diethyl ether (20 mL), and ethyl acetate (5 mL) to afford N-(3-{[3,5-bis(methoxy)phenyl]amino}quinoxalin-2-yl)-3-(2H-tetrazol-5-yl)benzenesulfonamide (55 mg, 25%) as light yellow solid. MS (EI) m/z for C23H20N8O4S: 505.0 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481001B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-6bbf2ec2accb46d4ac27f5aaa5332c6f |
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| Source note | uspto-grants-2013_07 |
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