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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111444Generated: November 1, 2026

Diisopropylethylamine → HCID 57635077, compound

https://huagongshe.com/reaction/2111444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-1-methylpiperidineHCID 2737531—
ReactantHCID 68737897HCID 68737897—
SolventDimethylformamideHCID 6228—
SolventSodium CarbonateHCID 10340—
ProductHCID 57635077HCID 57635077—

Reaction Steps

To a mixture of 3-methoxy-4-((R)-6-methyl-5-oxo-2,3,3a,4,5,6-hexahydro-1H-6,8,10,10b-tetraaza-benzo[e]azulen-9-ylamino)-benzoic acid (I-102a), 0.32 mL (0.0018 mole) of ethyldiisopropylamine and 0.082 g (0.00072 mole) of 4-amino-1-methyl-piperidine in 3.0 mL of dimethylformamide was added 0.31 g (0.00072 mole) of 1-(di-1-pyrrolidinylmethylene)-1H-benzotriazolium 3-oxide hexafluorophosphate. The mixture was stirred at room temperature for 3 hours, then diluted with saturated sodium carbonate. The mixture was extracted with ethyl acetate three times. The combined organic layers were dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Purification of the residue by silica gel chromatography, eluting with dichloromethane-methanol (100:0-60:40) gave 0.060 g of 3-methoxy-4-((R)-6-methyl-5-oxo-2,3,3a,4,5,6-hexahydro-1H-6,8,10,10b-tetraaza-benzo[e]azulen-9-ylamino)-N-(1-methyl-piperidin-4-yl)-benzamide (I-102).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517873B2
Source datasetuspto-grants-2009_04
ORD IDord-cb70ef25331a45268ae9aa1bf749eff3
Source noteuspto-grants-2009_04