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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488860Generated: November 4, 2026

Tert-butoxycarbonylalanine → HCID 22877896, compound

https://huagongshe.com/reaction/1488860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butoxycarbonylalanineHCID 85082—
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-enenitrile hydrochlorideHCID 9976854—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductHCID 22877896HCID 2287789680%

Reaction Steps

(E)-3-(3-Amino-4-methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)-prop-2-enenitrile hydrochloride (1,053 mg, 2.65 mmols), 1,300 mg of a BOP reagent and 554 mg of Boc-L-Ala were dissolved in 50 ml of acetonitrile, and 0.8 ml of triethylamine were added thereto. The mixture was reacted at 60° C. for 17 hours. One-hundred milliliters of water and a small amount (about 10 g) 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 dichloromethane and ethyl acetate at a ratio of 20:1), and then concentrated to produce 1,085 mg (2.12 mmols) of the final product in a yield of 80%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05674906
Source datasetuspto-grants-1997_10
ORD IDord-e0f0e0e4ace74e749050faf05b8838da
Source noteuspto-grants-1997_10