HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403645Generated: October 31, 2026
Sodium Cyanide → 4-[(1-Cyanocyclobutyl)amino]-2-fluoro-N-methylbenzamide
https://huagongshe.com/reaction/2403645
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Cyclobutanone | HCID 14496 | — |
| Reactant | 4-Amino-2-fluoro-N-methylbenzamide | HCID 44139521 | — |
| Product | 4-[(1-Cyanocyclobutyl)amino]-2-fluoro-N-methylbenzamide | HCID 44139520 | — |
Reaction Steps
A solution of 2,4-difluoro-benzoylchloride D in a solution of methylamine and tetrahydrofuran (THF) is allowed to react to produce 2,4-difluoro-N-methylbenzamide M (quantitative yield). The 2,4-difluoro-N-methylbenzamide M is mixed with in a solution of acetonitrile and 4-methoxy-benzenemethanamine and heated in a microwave for 20 minutes at 190° C. to produce 2-fluoro-4-(4-methoxybenzylamino)-N-methylbenzamide S (yield of 40%). The 2-fluoro-4-(4-methoxybenzylamino)-N-methylbenzamide S is reacted in a solution of dichloromethane and trifluoroacetic acid to produce 2-fluoro-4-amino-N-methylbenzamide T (yield greater than 95%). The 2-fluoro-4-amino-N-methylbenzamide T is reacted with a solution of sodium cyanide and cyclobutanone to produce 4-(1-cyanocyclobutylamino)-2-fluoro-N-methylbenzamide B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802689B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-ee513794efc449be92f37fea44133173 |
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| Source note | uspto-grants-2014_08 |
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