HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Iodophenylacetic acid → Methyl 2-(2-(4-iodophenyl)acetamido)-4-methylthiophene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Iodophenylacetic acid | HCID 137214 | — |
| Reactant | Methyl 2-amino-4-methylthiophene-3-carboxylate | HCID 2759773 | — |
| Product | Methyl 2-(2-(4-iodophenyl)acetamido)-4-methylthiophene-3-carboxylate | HCID 68755598 | 87% |
Reaction Steps
The title compound was synthesized in 87% yield according to protocol A from 2-(4-iodophenyl)acetic acid and methyl 2-amino-4-methylthiophene-3-carboxylate. 13C NMR (CDCl3) δ 167.5, 166.6, 149.8, 138.1, 134.8, 133.1, 131.4, 113.0, 112.3, 93.2, 51.5, 43.3, 17.8; MH+ 416.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073891B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-bb2b48de9ee8425589c93989a5fcc7c9 |
| Source note | uspto-grants-2015_07 |