HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784929Generated: October 30, 2026
HCID 4777624, compound → HCID 68956891, compound
https://huagongshe.com/reaction/1784929
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 4777624 | HCID 4777624 | — |
| Reactant | 1,3-Benzenedicarboxylic acid, monomethyl ester | HCID 6951279 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 68956891 | HCID 68956891 | 93% |
Reaction Steps
Et3N (1 drop, catalytic) was added to a stirred suspension of mono-Methyl isophthalate (0.294 mmol, 1.0 eq) in 2 ml SOCl2 under Ar. The mixture was heated to reflux at 90° C. for 2 h. The reaction was cooled to RT, and the solvent was removed in vacuo. The residue was placed under an Ar atmosphere and dissolved in 2 ml anh CH2Cl2. The resulting solution was treated with a solution of N-((4-methylthiazol-2-yl)methyl)propan-2-amine (0.294 mmol, 1.0 eq made from reductive amination of 4-methylthiazole-2-carbaldehyde with isopropylamine) dissolved in 1 ml anh CH2Cl2 under Ar. After stirring at RT for 30 min, the reaction was treated with ET3N (0.294 mmol, 1 eq). After stirring at RT for 30 min, the reaction is poured into a seperatory funnel, washed with sat. NaHCO3 (×1), water (×3), brine (×1), and dried over Na2SO4. The inorganics were removed via filtration, and the solvent was removed in vacuo yielding the crude product in 93% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07504420B2 |
|---|
| Source dataset | uspto-grants-2009_03 |
|---|
| ORD ID | ord-470f26b5a4894efe91e8c20c998849a6 |
|---|
| Source note | uspto-grants-2009_03 |
|---|