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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173168Generated: October 25, 2026

1,2-Dichloroethane → Benzyl 9-(5-{[(2-aminophenyl)amino]carbonyl}pyridin-2-yl)-3,9-diazaspiro[5.5]-undecane-3-carboxylate

https://huagongshe.com/reaction/1173168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantO-PhenylenediamineHCID 7243—
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantTert-butyl 9-[5-(methoxycarbonyl)pyridin-2-yl]-3,9-diazaspiro[5.5]undecane-3-carboxylateHCID 57717452—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
SolventMethanol tetrahydrofuran waterHCID 21892291—
ProductBenzyl 9-(5-{[(2-aminophenyl)amino]carbonyl}pyridin-2-yl)-3,9-diazaspiro[5.5]-undecane-3-carboxylateHCID 57717481—

Reaction Steps

A solution of tert-butyl 9-[5-(methoxycarbonyl)pyridin-2-yl]-3,9-diazaspiro[5.5]undecane-3-carboxylate (100 mg, 0.257 mmol) in 1 mL of CH2Cl2 and 1 mL of TFA was stirred for 1 h and concentrated. The oil was redissolved in 2 mL of CH2Cl2 and treated with NEt3 (0.15 mL, 1.08 mmol) and CbzCl (0.060 mL, 0.42 mmol), then stirred for 8 h. The mixture was partitioned between EtOAc and sat'd NaHCO3, dried (Na2SO4), filtered and concentrated. The residue was stirred in 3 mL of 1:1:1 MeOH/THF/water with LiOH.H2O (30 mg, 0.71 mmol) for 10 h, concentrated to dryness, dissolved in 2 mL of DMF, treated with EDC (150 mg, 0.79 mmol), HOBt (100 mg, 0.74 mmol), and phenylenediamine (100 mg, 0.93 mmol). The mixture was stirred for 18 h, concentrated, and triturated with methanol giving the title compound; MS (ESI+): cal'd [M+1]+ 500.3, obs'd 500.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834026B2
Source datasetuspto-grants-2010_11
ORD IDord-90dc515c8b344634b37c26f1088a0df6
Source noteuspto-grants-2010_11