HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → (Z)-2-(3,4-dimethoxy-phenyl)-3-(5-morpholin-4-yl-thiophen-2-yl)-acrylonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 3,4-Dimethoxybenzeneacetonitrile | HCID 66727 | — |
| Reactant | 5-Bromothiophene-2-carbaldehyde | HCID 78428 | — |
| Reactant | 5-(Morpholin-4-yl)thiophene-2-carboxaldehyde | HCID 2326306 | — |
| Product | (Z)-2-(3,4-dimethoxy-phenyl)-3-(5-morpholin-4-yl-thiophen-2-yl)-acrylonitrile | HCID 11965252 | 15% |
Reaction Steps
Through the procedure as employed in Production step 1, an amine moiety derived from morpholine (523 mg) was introduced into 5-bromothiophene-2-carboxaldehyde (382 mg), to thereby yield 5-morpholin-4-yl-thiophene-2-carbaldehyde (yield: 176 mg, 45%). The produced 5-morpholin-4-yl-thiophene-2-carbaldehyde (172 mg) was condensed with 3,4-dimethoxybenzyl cyanide (154 mg) through Method A (production step 2), to thereby yield the target product (yield: 46 mg, 15%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08697742B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-881f4219c35148faa1aaecdf11bf81ca |
| Source note | uspto-grants-2014_04 |