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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978190Generated: November 1, 2026

Sodium hydride → HCID 21996872, compound

https://huagongshe.com/reaction/1978190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 21996882HCID 21996882—
ReactantHCID 178428694HCID 178428694—
SolventHexaneHCID 8058—
ProductHCID 21996872HCID 2199687271.7%

Reaction Steps

Sodium hydride (60% suspension in oil, 0.25 g, 6.25 mmol) was washed with hexane, dried under nitrogen and resuspended in dry dimethylformamide (10 mL). Neat 3-methylpyrazole (0.28 mL, 3.5 mmol) was added in one portion at ambient temperature. Stirring was continued until the gas evolution subsided. The (5-fluoro-2-(methyl)-phenyl)-(6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepin-6-yl)-methanone of Step B (0.75 g, 1.94 mmol) was added in one portion to the clear solution. The mixture was heated to reflux for 26 hours, cooled and partitioned between water and ethyl acetate. The organic extracts were dried over sodium sulfate and evaporated to dryness. The residue was dissolved in dichloromethane and absorbed onto a silica Merck-60 flash column. Elution with hexane-ethyl acetate (gradient from 8:2 to 7:3) provided the title product (0.55 g) as a pale yellow foam which was crystallized by sonication from hexane-ethanol, m.p. 209-210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235900B1
Source datasetuspto-grants-2001_05
ORD IDord-fe64795d6d5441e39eb45a00f3f0bf3d
Source noteuspto-grants-2001_05