HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243760Generated: October 26, 2026
Ammonia → 4-Chloro-2-(3-aminomethyl-2-methysulfanyl-phenoxy)-benzonitrile fumarate
https://huagongshe.com/reaction/1243760
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | 4-Chloro-2-(3-chloromethyl-2-methysulfanyl-phenoxy)-benzonitrile | HCID 21930442 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Chloro-2-(3-aminomethyl-2-methysulfanyl-phenoxy)-benzonitrile fumarate | HCID 69423376 | — |
Reaction Steps
7N Ammonia in methanol (30 mL, 210 mmol) was added to 4-chloro-2-(3-chloromethyl-2-methysulfanyl-phenoxy)-benzonitrile (240 mg, 0.8 mmol). After stirring for 17 h, TLC still showed some 4-chloro-2-(3-chloromethyl-2-methysulfanyl-phenoxy)-benzonitrile. The reaction mixture was concentrated to about 10 mL by evaporation in vacuo, concentrated ammonia (7 mL) was added and the mixture was heated with stirring at 60° C. for 17 h. Sodium carbonate solution (4 mL) and ethyl acetate (6 mL) were added and the organic layer was separated and dried with MgSO4. To this, was added fumaric acid (84 mg, 0.64 mmol) in methanol (3 mL). Immediately, the solvent was removed in vacuo and diethyl ether (40 mL) was added to the residue. After stirring for 17 h, 4-chloro-2-(3-aminomethyl-2-methysulfanyl-phenoxy)-benzonitrile fumarate (134.7 mg, 53%) was filtered off as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119122B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-266b3bc613b04a158bd8b746845f5821 |
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| Source note | uspto-grants-2006_10 |
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