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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873036Generated: October 29, 2026

Water → 2,3,4,4a,9,9a-Hexahydro-1H-indeno(2,1-b)pyridine-6-carbonitrile

https://huagongshe.com/reaction/873036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridine-6-carboxamideHCID 71264365—
Solvent1,4-DioxaneHCID 31275—
Product2,3,4,4a,9,9a-Hexahydro-1H-indeno(2,1-b)pyridine-6-carbonitrileHCID 67195070—

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridine-6-carboxamide (I), hydrogen chloride salt (7.5 Kg, 25.2 mol) and dioxane (15 L) is stirred for 30 minutes at 25° C. and treated with POCl3 (7.77 Kg, 50.4 mol). The mixture is heated to 80° C. over 1 hour and held at 80° C. for 2 hours. The mixture is cooled to 20-25° C., treated over about 30 minutes with a solution of water (1.376 L, 75.6 mol) in dioxane (30 L), stirred for 30 minutes, and treated with additional water (1.376 L, 75.6 mol). The resulting slurry is stirred at 25° C. for about 18 hours and filtered. The resulting filter cake is washed portion-wise with 3.0 L of 1% H2O in 1,4-dioxane and dried for about 18 hours at ˜50° C. to provide 2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridine-6-carbonitrile (III) in the form of the hydrogen chloride salt. Yield: 4.73 Kg, 20.16 mol; 80%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975405B2
Source datasetuspto-grants-2015_03
ORD IDord-1b41c2ba8bb84b9dbf2da3f7aaeef945
Source noteuspto-grants-2015_03