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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890710Generated: October 31, 2026

Ammonium Hydroxide → HCID 58550623, compound

https://huagongshe.com/reaction/1890710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 58550577HCID 58550577—
CatalystHCID 178511488HCID 178511488—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 58550623HCID 58550623—

Reaction Steps

To a rapidly stirred solution of (2S)-2′-oxo-1′-{[2-(trimethylsilyl)eth-oxy]methyl}-1,1′,2′,3-tetrahydrospiro[cyclopenta[b]quinoline-2,3′-pyrrolo[2,3-b]pyridine]-7-carbohydrazide from Step H (317 mg, 0.667 mmol) in DCM (6.8 mL) was added water (2.7 mL) plus concentrated aqueous NH4OH (0.6 mL) and lastly potassium ferricyanide (549 mg, 1.67 mmol). After 4.5 hours the reaction was diluted with water (20 mL) and DCM (40 mL). The aqueous layer was extracted once with DCM (20 mL). The combined organics were washed successively with water then half-saturated brine and then dried over sodium sulfate. The organics were then filtered, concentrated in vacuo, and applied to a silica gel column for purification, eluting with a gradient of CH2Cl2:MeOH—99:1 to 90:10. Clean product-containing fractions were pooled and concentrated in vacuo to give the title compound. MS: m/z=446 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507477B2
Source datasetuspto-grants-2013_08
ORD IDord-fac5351aa7804aa2bbc8b30e6fc12639
Source noteuspto-grants-2013_08