HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 5-(2-Chlorobenzyl)-4-methoxymethyl-9-tosyl-beta-carboline-3-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 5-(4-Chlorobenzyl)-4-methoxymethyl-beta-carboline-3-carboxylic acid ethyl ester | HCID 54002862 | — |
| Product | 5-(2-Chlorobenzyl)-4-methoxymethyl-9-tosyl-beta-carboline-3-carboxylic acid ethyl ester | HCID 53990242 | — |
Reaction Steps
0.744 g (0.0039 mol) of p-toluenesulfochloride is added under ice cooling to a solution of 1.2 g (0.0029 mol) of 5-(4-chlorobenzyl)-4-methoxymethyl-β-carboline-3-carboxylic acid ethyl ester, 0.16 g (0.0013 mol) of dimethylaminopyridine and 0.54 ml (0.0039 mol) of triethylamine in 120 ml of dichloromethane. The reaction mixture is stirred for another 15 minutes under ice cooling and then for 2 hours at room temperature. Then it is diluted with dichloromethane, washed with water, dried and concentrated by evaporation. The evaporation residue is crystallized under trituration with ether. The yield is 1.36 g (82% of theory) of 5-(2-chlorobenzyl)-4-methoxymethyl-9-tosyl-β-carboline-3-carboxylic acid ethyl ester, melting point 140°-142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05506234 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-abc7e3116cf34163aa8095bd0ae078c7 |
| Source note | uspto-grants-1996_04 |