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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868807Generated: October 31, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 86690206, compound

https://huagongshe.com/reaction/868807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantChloromethyl chloroformateHCID 62754—
ReactantOlanzapineHCID 135398745—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86690206HCID 8669020686.4%

Reaction Steps

To a solution of olanzapine (5.0 g, 16 mmol) in tetrahydrofuran (50 mL) at −78° C. was added tetramethylethylenediamine (2.4 mL, 16 mmol), followed by 2M n-BuLi in hexanes (8.0 mL, 16 mmol) over 5 min. The reaction mixture was stirred for 15 min and then chloromethyl chloroformate (2.1 mL, 24 mmol) added and the reaction mixture stirred a further 30 min. The reaction mixture was then warmed to room temperature, stirred for 1 h and quenched with water (50 mL). This mixture was diluted with brine (50 mL) and extracted with ethyl acetate (50 mL). The organic phase was dried over MgSO4, evaporated and the residue further purified by column chromatography on silica eluting with 0.2:1:1 methanol/dichloromethane/ethyl acetate to give chloromethyl 2-methyl-4-(4-methylpiperazin-1-yl)-10H-benzo[b]thieno[2,3-e][1,4]diazepine-10-carboxylate [C] (5.6 g, ˜50% pure by 1H NMR and LCMS). This was used directly in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969337B2
Source datasetuspto-grants-2015_03
ORD IDord-855fe6ea138748f8b7ef3738cb46c918
Source noteuspto-grants-2015_03