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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350440Generated: October 31, 2026

Formaldehyde → (s)-2-Methyl-10-[4-methyl-3-(2-thiophen-3-yl-ethyl)-piperazin-1-yl]-4h-3-thia-4,9-diaza-benzo[f]azulene dihydrochloride

https://huagongshe.com/reaction/1350440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantDichloromethaneHCID 6344—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 135932169HCID 135932169—
SolventSodium BicarbonateHCID 516892—
Product(s)-2-Methyl-10-[4-methyl-3-(2-thiophen-3-yl-ethyl)-piperazin-1-yl]-4h-3-thia-4,9-diaza-benzo[f]azulene dihydrochlorideHCID 13646446959%

Reaction Steps

Add formaldehyde (45 μL, 0.56 mmol, 37% in water) to a solution of (S)-2-methyl-10-[3-(2-thiophen-3-yl-ethyl)-piperazin-1-yl]-4H-3-thia-4,9-diaza-benzo[f]azulene (210 mg, 0.51 mmol) in methylene chloride (6 mL). Stir 15 min at ambient temperature. Add sodium triacetoxyborohydride (163 mg, 0.77 mmol) and stir 2h at ambient temperature. Dilute with saturated sodium bicarbonate solution and extract with methylene chloride. Dry the extracts with sodium sulfate, filter and concentrate the filtrate. Purify by radial silica gel chromatography using a 2 mm plate and 2N ammonia in methanol-methylene chloride (2%) as the eluent to give 127 mg (59%) of the free base of the title compound. Crystallize the dihydrochloride salt from ethyl acetate and ethanol to give the title compound: mass spectrum (ion spray): m/z=423 (M+1), 421 (M−1). Analysis calculated for C23H28Cl2N4S2.0.2HCl.0.3H2O: C, 54.35; H, 5.71; N, 11.01; Cl, 15.35. Found: C, 54.10; H, 5.34; N, 10.99; Cl, 15.00. HR-MS calculated for C23H27N4S2423.1677. Found 423.1656.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214673B2
Source datasetuspto-grants-2007_05
ORD IDord-303da1b1af594f3c96076aaf2ba31b40
Source noteuspto-grants-2007_05