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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519474Generated: November 3, 2026

Pyridine → HCID 66733393, compound

https://huagongshe.com/reaction/1519474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloromethyl chloroformateHCID 62754—
ReactantTolvaptanHCID 216237—
SolventDichloromethaneHCID 6344—
ProductHCID 66733393HCID 66733393—

Reaction Steps

Tolvaptan (5.0 g) and pyridine (1.1 ml) were suspended in dichloromethane (50 ml). Chloromethyl chloroformate (1.1 ml) was added thereto under cooling with ice, and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was washed with water, dried over anhydrous sodium sulfate. After filtration and concentration under reduced pressure, the residue was purified by silica gel flash chromatography (n-hexane:ethyl acetate=70:30→50:50). The purified product was concentrated under reduced pressure to obtain 6.1 g of chloromethyl {7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl} carbonate as white amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073868B2
Source datasetuspto-grants-2015_07
ORD IDord-ea11afe405f4423582aebe1afb4f39e9
Source noteuspto-grants-2015_07