HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583101Generated: October 30, 2026
4-Methylmorpholine → N-[3-Cyano-4-[[(dimethylamino)methylene]amino]phenyl]-2-butynamide
https://huagongshe.com/reaction/583101
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 2-Butynoic acid | HCID 68535 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (E)-N'-(4-Amino-2-cyanophenyl)-N,N-dimethylformimidamide | HCID 11263933 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | N-[3-Cyano-4-[[(dimethylamino)methylene]amino]phenyl]-2-butynamide | HCID 18350692 | 89% |
Reaction Steps
To a solution of 2.01 g (23.9 mmol) of 2-butynoic acid and 2.9 ml (22.3 mmol) isobutyl chloroformate in 30 ml tetrahydrofuran was stirred at 0° C. under nitrogen as 2.42 g (2.63 ml, 22.3 mmol) of N-methyl morpholine was added over 3 min. After stirring for 15 min., a solution of N'-(4-amino-2-cyanophenyl)-N,N-dimethylformamidine and 1.6 g (1.75 ml, 15.9 mmol) of N-methyl morpholine in 25 ml tetrahydrofuran was added over 4 min. The mixture was stirred 30 min. at 0° C. and 30 min. at room temperature. The mixture was diluted with 70 ml of ethyl acetate and poured into a mixture of brine and saturated sodium bicarbonate. The organic layer was dried (MgSO4) and filtered through a pad of silica gel. The solvent was removed and the residue was stirred with 50 ml of ether. The suspended solid was collected to give 3.61 g (89%) of an off-white solid. mass spectrum (m/e): 255.0 (M+H, electrospray).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05929080 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-07a9a542b1654bb29ad329e06359b547 |
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| Source note | uspto-grants-1999_07 |
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