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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574646Generated: October 29, 2026

Methyl chloroformate → HCID 71515726, compound

https://huagongshe.com/reaction/574646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 71515995HCID 71515995—
SolventDichloromethaneHCID 6344—
ProductHCID 71515726HCID 7151572656%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

According to Scheme 11: To a solution of 3-[1-((1R,2R)-4,6-difluoro-2-hydroxy-indan-1-yl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-3-yl]-benzonitrile (11t) (0.05 g, 0.123 mmol) in dry CH2Cl2 (2 ml) at 0° C. methyl chloroformate (12 mg, 0.13 mmol) and NEt3 (19 mg, 0.191 mmol) was added, the mixture was stirred at 0-5° C. for 60 min, then at 25° C. for 18 h. After addition of aqueous saturated NaHCO3 (2 ml), the mixture was extracted with CH2Cl2 (10 ml), the organic layer was dried over Na2SO4, solvents were evaporated in vacuo and the crude product was purified by purified by reverse phase HPLC (CH3CN/water gradient with 0.1% trifluoroacetic acid) to give 31 mg of 3-(3-cyano-phenyl)-1-((1R,2R)-4,6-difluoro-2-hydroxy-indan-1-yl)-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridine-5-carboxylic acid methyl ester (17a).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034897B2
Source datasetuspto-grants-2015_05
ORD IDord-c87844c08d9c4e1a92c641f32cb6387f
Source noteuspto-grants-2015_05