HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 6-chloro-N-(4-iodo-3-methyl-phenyl)-nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Iodo-3-methylaniline | HCID 2734275 | — |
| Reactant | 6-Chloronicotinoyl Chloride | HCID 2782165 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-chloro-N-(4-iodo-3-methyl-phenyl)-nicotinamide | HCID 59318138 | 86% |
Reaction Steps
A solution of 3-methyl-4-iodoaniline (660 mg 2.84 mmol), diisopropylethyl amine (1.2 mL 8.52 mmol) and a catalytic amount of DMAP in CH2Cl2 (15 mL) was treated with 6-chloronicotinoyl chloride (500 mg, 2.84 mmol). Upon completion of the reaction, as judged by TLC, the mixture was partitioned between CH2Cl2 and water. The EtOAc layer was dried over Na2SO4 filtered and concentrated. The solid residue was washed with hexanes and then was passed through a silica gel plug with 50% EtOAc in hexanes as the elution solvent to afford the product, 6-chloro-N-(4-iodo-3-methyl-phenyl)-nicotinamide. (910 mg, Yield 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08324385B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-170db9a435624e4ea45c95cc4881aedf |
| Source note | uspto-grants-2012_12 |