HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → N-((R)-5-Bromoindan-2-yl)-4-butoxy-N-methylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Butoxybenzoyl chloride | HCID 118561 | — |
| Reactant | 1H-Inden-2-amine, 5-bromo-2,3-dihydro-, (2R)- | HCID 11275870 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-((R)-5-Bromoindan-2-yl)-4-butoxy-N-methylbenzamide | HCID 66679860 | — |
Reaction Steps
A mixture of (R)-5-bromoindan-2-ylamine (hydrochloride; 3.50 g), diisopropylethylamine (5.0 ml) and dichloromethane (20 ml) was admixed at 0° C. with 4-butoxybenzoyl chloride (3.00 g). After 30 minutes, the reaction mixture was partitioned between water and dichloromethane. The organic phase was concentrated and the residue was stirred with diethyl ether. The resulting amide was methylated on the amide nitrogen according to method D. This afforded the product with the molecular weight of 402.33 (C21H24BrNO2); MS (ESI): 402 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552199B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-50aaa5ee56104e12b4c964dbe13c2bee |
| Source note | uspto-grants-2013_10 |