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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725421Generated: October 29, 2026

Sodium Hydroxide → HCID 67338376, compound

https://huagongshe.com/reaction/1725421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium AzideHCID 33557—
ReactantHCID 12524226HCID 12524226—
ProductHCID 67338376HCID 6733837668%
ProductHCID 67340437HCID 6734043718%

Reaction Conditions

Temperature90 °C

Reaction Steps

Add 1,2,5,6-tetrahydropyrrolo[3,2,1-ij]quinolin-6-one (15.49 g, 89.43 mmol) to polyphosphoric acid (512 g) at 67-70° C. and stir vigorously. Add three portions of sodium azide (2.43 g (37.4 mmol), 2.42 g (37.2 mmol) and 2.42 g (37.2 mmol)) at 20 minute intervals then heat to 90° C. and stir for 3.5 hours. Pour into ice (511.6 g). Add, with cooling, 50% aqueous sodium hydroxide (500 mL) 40 minutes. Extract with chloroform (3×500 mL). Wash the combined organic phases with water (500 mL) and saturated aqueous sodium chloride (500 mL). Dry over sodium sulfate and concentrate under reduced pressure. Subject the residue to chromatography (pre-packed silica gel), eluting with a gradient: 98:2-97:3-96:4 chloroform/methanol to provide 1,2,4,5-tetrahydro-7H-[1,4]diazepino[3,2,1-hi]indol-6-one (2.95 g, 18%) and 1,2,4,5-tetrahydro-6H-[1,4]diazepino[6,7,1-hi]indol-7-one (11.51 g, 68%) as beige solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491716B2
Source datasetuspto-grants-2009_02
ORD IDord-a73ddd7bd5c14652b78b0c68a12bd060
Source noteuspto-grants-2009_02