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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468791Generated: November 3, 2026

Phenyl chloroformate → HCID 136350277, compound

https://huagongshe.com/reaction/1468791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl chloroformateHCID 15891—
ReactantHCID 67977664HCID 67977664—
ReactantHCID 68160332HCID 68160332—
ProductHCID 136350277HCID 136350277—

Reaction Steps

Phenyl (2R)-2-(1-methyl-6-oxo-1,6-dihydro-[4,4]bipyrimidinyl-2-yloxymethyl)pyrrolidine-1-carboxylate was prepared by the same manner as that of methyl 3-(1-methyl-6-oxo-1,6-dihydro-[4,4′]bipyrimidinyl-2-yloxy)piperidine-1-carboxylate except for utilizing (R)-1-methyl-2-(pyrrolidin-2-ylmethoxy)-1H-[4,4′]bipyrimidinyl-6-one (0.20 g, 0.70 mmol) instead of 1-methyl-2-(piperidine-3-yloxy)-1H-[4,4′]bipyrimidinyl-6-one and phenyl chloroformate (125 μl, 1.0 mmol) instead of methyl chloroformate. Phenyl (2R)-2-(1-methyl-6-oxo-1,6-dihydro-[4,4′]bipyrimidinyl-2-yloxymethyl)pyrrolidine-1-carboxylate was isolated as a white solid (29 mg, 0.07 mmol, 10%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006232B2
Source datasetuspto-grants-2015_04
ORD IDord-11c7476ca0804006879dbe894772a418
Source noteuspto-grants-2015_04