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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489577Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 10303235, compound

https://huagongshe.com/reaction/489577

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(Methylamino)propane-1,2-diolHCID 2734122—
ReactantHCID 10299280HCID 10299280—
ReactantEthylcarbodiimide hydrochlorideHCID 21883477—
SolventEthyl AcetateHCID 8857—
ProductHCID 10303235HCID 1030323591.4%

Reaction Steps

10-(5-Chloro-4-cyclohex-1-en-1-yl-2-methoxybenzoyl)-10,11-dihydro-5H-pyrrolo [2,1-c][1,4]benzodiazepine-3-carboxylic acid of Example 1, Step G (0.370 g, 0.776 mmol), 3-methylamino-1,2-propanediol (0.098 g, 0.931 mmol), 1-hydroxy benzotriazole (0.115 g, 0.854 mmol) and 1-[3-dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (0.164 g, 0.854 mmol) were combined in amine-free N,N-dimethylformamide (3.9 mL), followed by addition of N,N-diisopropylethylamine (0.202 mL, 1.16 mmol). The reaction was stirred at room temperature for 12 hours, then diluted with ethyl acetate and washed with 1 N hydrochloric acid, 1 N sodium hydeoxide and brine. The combined aqueous washings were saturated with sodium chloride and extracted with ethyl acetate. The combined organic phases were dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was purified by flash column chromatography on silica gel eluting with a solvent gradient from 0 to 5% of methanol in chloroform, to afford 0.400 g of the title compound as a white, crystalline solid, m.p.155-157° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06977254B2
Source datasetuspto-grants-2005_12
ORD IDord-c44892696c5c442f83b75cce3d6ad11c
Source noteuspto-grants-2005_12