HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387378Generated: October 31, 2026
4-Nitrophenyl chloroformate → HCID 22725170, compound
https://huagongshe.com/reaction/1387378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | HCID 178436961 | HCID 178436961 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22725170 | HCID 22725170 | 92% |
Reaction Steps
To a well stirred solution of (+)-5-(benzyloxycarbonyl) -1,6-dihydro-2-methoxy-4-ethyl-6-(2,4-difluorophenyl) pyrimidine (4.1 g, 10.62 mmol) and 4-(N,N-dimethylamino)pyridine (1.69 g, 13.80 mmol) in CH2Cl2 (200 mL) was added a powder of 4-nitrophenyl chloroformate (2.78 g, 13.80 mmol) at room temperature. The reaction mixture was stirred for 12 h and washed with 0.5 N NaOH solution (2×50 mL). The organic layer was separated and dried (Na2SO4). The solvent was evaporated and the residue was purified by column chromatography on silica gel using dichloromethane/hexane (20%-50%) as the eluent to give (+)-5-(benzyloxycarbonyl)-4-ethyl-1,6-dihydro-2-methoxy-6-(2,4-difluorophenyl)-1-[(4-nitrophenyloxy)carbonyl]pyrimidine (5.37 g, 92%) as a viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06268369B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-369a0f47172d4de2b89d3852cb944166 |
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| Source note | uspto-grants-2001_07 |
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