HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 66798963, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 2-(bromomethyl)-6-chlorobenzoate | HCID 22935208 | — |
| Reactant | HCID 66799167 | HCID 66799167 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66798963 | HCID 66798963 | — |
Reaction Steps
2-Bromomethyl-6-chlorobenzoic acid methyl ester (1.689 mmol, 1.0 eq) was dissolved in toluene (5.2 ml) and triethylamine (2.534 mmol, 1.5 eq), and (R)-methyl 4-aminochromane-7-carboxylate (A-04) (1.689 mmol, 1 eq) was added. The reaction mixture was refluxed for 16 h and then diluted with water and dichloromethane. The phases were separated and the aqueous phase was extracted with dichloromethane (2×). The organic phases were washed with sat. NaCl solution, dried over magnesium sulfate and concentrated. The crude product was purified by column chromatography (silica gel, cyclohexane:EA 3:1), and the desired product (R)-methyl 4-(7-chloro-1-oxoisoindolin-2-yl)chromane-7-carboxylate (D-03) was thus obtained. Yield: 60%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680159B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-1316cea81d4e4226ba193fedd2f09ff5 |
| Source note | uspto-grants-2014_03 |