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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350513Generated: October 30, 2026

Formaldehyde → 11-{(S)-3-[2-(3-Fluoro-phenyl)-ethyl]-4-methyl-piperazin-1-yl}-3-methyl-5H-dibenzo[b,e][1,4]diazepine

https://huagongshe.com/reaction/1350513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant11-{(S)-3-[2-(3-Fluoro-phenyl)-ethyl]-piperazin-1-yl}-3-methyl-5H-dibenzo[b,e][1,4]diazepineHCID 58860720—
Solvent1,2-DichloroethaneHCID 11—
Product11-{(S)-3-[2-(3-Fluoro-phenyl)-ethyl]-4-methyl-piperazin-1-yl}-3-methyl-5H-dibenzo[b,e][1,4]diazepineHCID 5886057892%

Reaction Steps

Combine 11-{(S)-3-[2-(3-fluoro-phenyl)-ethyl]-piperazin-1-yl}-3-methyl-5H-dibenzo[b,e][1,4]diazepine (385.5 mg, 0.93 mmol), formaldehyde (83.0 μL, 1.02 mmol, 37% in water), and 1,2-dichloroethane (30.0 ml). Stir the mixture at ambient temperature for 5 minutes and then add sodium triacetoxyborohydride (295.6 mg, 1.39 mmol). After stirring for 30 minutes at ambient temperature, quench the reaction with saturated sodium bicarbonate. Remove the organic portion and wash (brine), dry (sodium sulfate), and reduce the extracts to residue. Purify the residue on silica gel using dichloromethane/methanol (90:10) to give 366.2 mg (92%) of the title compound as a yellow foam: mp 63°, dec; mass spectrum (ion spray): m/z=429.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214673B2
Source datasetuspto-grants-2007_05
ORD IDord-9049378ad7d6486fa0f36d2a5c2f003d
Source noteuspto-grants-2007_05