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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488866Generated: November 3, 2026

1-Hydroxybenzotriazole → HCID 178490140, compound

https://huagongshe.com/reaction/1488866

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantSodium BicarbonateHCID 516892—
Reactant(E)-3-(3-amino-4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-prop-2-enenitrileHCID 9840884—
Reactant(2S)-4-(Benzyloxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-oxobutanoic acidHCID 13966931—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductHCID 178490140HCID 178490140135.8%

Reaction Steps

Nine-hundred milligrams (2.65 mmols) of (E)-3-(3-amino-4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-prop-2-enenitrile, 1,400 mg of Fmoc-L-Asp(OBn), 1,300 mg of a BOP reagent and 660 mg of HOBt.H2O were dissolved in 50 ml of acetonitrile, and 0.5 ml of triethylamine were added thereto. The mixture was reacted at room temperature for 86 hours. One-hundred milliliters of water and a small amount of sodium hydrogencarbonate were added thereto, and the resulting mixture was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The product was purified using a silica-gel column (eluent, mixture of ethyl acetate and dichloromethane at a ratio by volume of 1:10), and then concentrated to give 1,319 mg (1.80 mmols) of the final product in a yield of 68%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05674906
Source datasetuspto-grants-1997_10
ORD IDord-9749be6281d0440ba596b352b549aafc
Source noteuspto-grants-1997_10