HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-1-(5-bromothiophen-2-yl)ethan-1-one → 4-[4-(5-Bromo-thiophen-2-yl)-thiazol-2-yl]-2'-nitro-biphenyl-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-1-(5-bromothiophen-2-yl)ethan-1-one | HCID 1988398 | — |
| Reactant | 2'-Nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl ester | HCID 86679832 | — |
| Product | 4-[4-(5-Bromo-thiophen-2-yl)-thiazol-2-yl]-2'-nitro-biphenyl-2-carboxylic acid | HCID 71536631 | 33% |
Reaction Steps
4-[4-(5-Bromo-thiophen-2-yl)-thiazol-2-yl]-2′-nitro-biphenyl-2-carboxylic acid (180 mg, 33%) was prepared from 2′-nitro-4-thiocarbamoyl-biphenyl-2-carboxylic acid methyl ester (which may be prepared as described for Intermediate 4) and 2-bromo-1-(5-bromothiophen-2-yl)ethanone (available from Oakwood Products, Inc.) using the procedure described for the preparation of Example 1. 1H NMR (300 MHz, DMSO-d6) δ 13.16 (s, 1H), 8.50 (d, J=1.8 Hz, 1H), 8.13-8.22 (m, 3H), 7.52 (d, J=3.9 Hz, 1H), 7.40-7.48 (m, 2H), 7.28 (d, J=3.9 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073881B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-986348c0c53a4cb4a5c4314be947742f |
| Source note | uspto-grants-2015_07 |