HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Formyl-4-methylthiophene-2-carboxylic acid → Rac-5-{3-[4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-3,5-dimethyl-phenyl]-[1,2,4]oxadiazol-5-yl}-3-methyl-thiophene-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Formyl-4-methylthiophene-2-carboxylic acid | HCID 53212682 | — |
| Reactant | HCID 178426655 | HCID 178426655 | — |
| Product | Rac-5-{3-[4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-3,5-dimethyl-phenyl]-[1,2,4]oxadiazol-5-yl}-3-methyl-thiophene-2-carbaldehyde | HCID 87330589 | — |
Reaction Steps
The title compound is prepared according to Method A starting from 5-formyl-4-methyl-thiophene-2-carboxylic acid and rac-4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-N-hydroxy-3,5-dimethyl-benzamidine; LC-MS: tR=1.16 min; [M+1]+=429.16; 1H NMR (D6-DMSO): δ1.34 (s, 3H), 1.38 (s, 3H), 2.34 (s, 6H), 2.65 (s, 3H), 3.79-3.93 (m, 3H), 4.10-4.15 (m, 1H), 4.42-4.49 (m, 1H), 7.75 (s, 2H), 8.07 (s, 1H), 10.17 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08148410B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-609d6a38ace44c37afa337bbc1939ebd |
| Source note | uspto-grants-2012_04 |