HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746793Generated: October 31, 2026
Methyl chloroformate → HCID 59447046, compound
https://huagongshe.com/reaction/1746793
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-[Cyclohexyl(cyclopropylmethyl)amino]pyrimidine-4-carboxylic acid | HCID 59446841 | — |
| Reactant | HCID 59446860 | HCID 59446860 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59447046 | HCID 59447046 | — |
Reaction Steps
A cooled (0° C.) solution of 6-(cyclohexyl(cyclopropylmethyl)amino)pyrimidine-4-carboxylic acid (Intermediate 13, 130 mg; 0.47 mmol) in DCM was treated with diisopropylamine (90 mL; 0.52 mmol) and methyl chloroformate (40 mL; 0.52 mmol). After stirring at 0° C. for 15 minutes, ethyl 3-(4-aminobenzylsulfonyl)propanoate (Intermediate 42, 130 mg; 0.48 mmol) was added. After stirring at 0° C. for 30 minutes and RT for 1 hour, saturated sodium bicarbonate solution was added and the mixture stirred for 15 minutes. DCM was added and the layers separated. The organic extract was filtered through a hydrophobic frit and the solvent removed in vacuo. The residue was purified by column chromatography (silica) eluting with petroleum ether containing increasing amounts of EtOAc to give the title compound as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09150519B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-c3c90fbe7ba2442cb13d9e0e568c7ee7 |
|---|
| Source note | uspto-grants-2015_10 |
|---|