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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220798Generated: October 30, 2026

4-Nitrobenzyl chloroformate → [4-(3,6-Dimethyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulene-9-carbonyl)-cyclohexylmethyl]-carbamic Acid 4-nitro-benzyl Ester

https://huagongshe.com/reaction/220798

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzyl chloroformateHCID 78205—
Reactant(4-Aminomethyl-cyclohexyl)-(3,6-dimethyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulen-9-yl)-methanone hydrochlorideHCID 136346633—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product[4-(3,6-Dimethyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulene-9-carbonyl)-cyclohexylmethyl]-carbamic Acid 4-nitro-benzyl EsterHCID 136128416—

Reaction Steps

A solution of 4-nitrobenzyl chloroformate (1.08 mg, 0.005 mmol) in dichloromethane (0.05 ml) was added to a solution of (4-Aminomethyl-cyclohexyl)-(3,6-dimethyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulen-9-yl)-methanone hydrochloride (Compound number 149) (1.95 mg, 0.005 mmol) in dichloromethane (0.05 ml) and triethyl-amine (0.0035 ml). The mixture was stirred at room temperature for 1 h then solvents were removed in vacuo to yield the title compound. (ESI)+: [M+H]+=533.3

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202858B2
Source datasetuspto-grants-2012_06
ORD IDord-5adf79b98eea42ada7369bada0e6a2b1
Source noteuspto-grants-2012_06