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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482947Generated: October 30, 2026

rac-(1R,2S)-N1,N2-dimethylcyclohexane-1,2-diamine → tert-butyl 1-isopropyl-7-(methylsulfonyl)-3,4-dihydrobenzo[4,5]imidazo[1,2-a]pyrazine-2(1H)-carboxylate

https://huagongshe.com/reaction/1482947

Reaction equation

Participants

RoleNameHCIDCharge
Reactantrac-(1R,2S)-N1,N2-dimethylcyclohexane-1,2-diamineHCID 7020757—
Reactant2-Bromo-4-methanesulfonylanilineHCID 20134402—
ReactantHCID 67492477HCID 67492477—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Producttert-butyl 1-isopropyl-7-(methylsulfonyl)-3,4-dihydrobenzo[4,5]imidazo[1,2-a]pyrazine-2(1H)-carboxylateHCID 8981561434%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of tert-butyl 2-isopropyl-3-oxopiperazine-1-carboxylate (200 mg, 0.83 mmol) in NMP (3 mL) was added 2-bromo-4-(methylsulfonyl)aniline (207 mg, 0.83 mmol), (1R,2S)—N1,N2-dimethylcyclohexane-1,2-diamine (12.0 mg, 0.08 mmol), K3PO4.3H2O (660 mg, 2.48 mmol), Cul (16 mg, 0.08 mmol). The mixture was stirred at 150° C. for 1 h under microwave. The mixture was diluted with water (10 mL) and extracted with EtOAc (3×10 mL). The combined organic layers were washed with brine (10 mL), dried over anhydrous Na2SO4, filtered, concentrated and purified by preparative TLC with CH2Cl2/MeOH 35/1 to afford tert-butyl 1-isopropyl-7-(methylsulfonyl)-3,4-dihydrobenzo[4,5]imidazo[1,2-a]pyrazine-2(1H)-carboxylate (110 mg, 34% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416135B2
Source datasetuspto-grants-2016_08
ORD IDord-56527dd893b548259f300cfbb0a1eff5
Source noteuspto-grants-2016_08