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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643106Generated: October 28, 2026

4-Nitrophenyl chloroformate → HCID 67273366, compound

https://huagongshe.com/reaction/643106

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant3-(Piperidin-4-yl)-4,5-dihydro-1H-benzo[d][1,3]diazepin-2(3H)-oneHCID 11379587—
Reactantmethyl(R)-3-(4-benzyloxy-3,5-dimethyl-phenyl)-2-hydroxy-propionateHCID 67273374—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
ProductHCID 67273366HCID 67273366—

Reaction Steps

Under a nitrogen atmosphere 1.93 g (9.58 mmol) 4-nitrophenyl chloroformate was added to a solution of 1.17 g (9.58 mmol) 4-dimethylaminopyridine in 50 mL pyridine, stirred for 1.5 h at RT, combined with 3.0 g (9.58 mmol) methyl (R)-3-(4-benzyloxy-3,5-dimethyl-phenyl)-2-hydroxy-propionate and stirred for 20 min at RT. Then 2.35 g (9.58 mmol) 3-piperidin-4-yl-1,3,4,5-tetrahydro-1,3-benzodiazepin-2-one were added and the mixture was stirred for 20 h at RT. The reaction mixture was evaporated down i.vac., the residue was taken up in EtOAc, the organic phase was washed with 10% KHSO4 and saturated NaHCO3 solution and dried over Na2SO4. After the desiccant and solvent had been eliminated the residue was purified by chromatography (silica gel, gradient Cyc/EtOAc 1:1 to 1:2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696209B2
Source datasetuspto-grants-2010_04
ORD IDord-77caa5ed426d4c08a55a4d9ef3a653ad
Source noteuspto-grants-2010_04