Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492908Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 57677333, compound

https://huagongshe.com/reaction/492908

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantN-((1,1-dimethylethoxy)carbonyl)-beta-alanineHCID 76809—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantAzetidine hydrochlorideHCID 12308726—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 57677333HCID 5767733399.4%

Reaction Steps

After adding azetidine hydrochloride (2.96 g) to a solution of triethylamine (4.42 ml) in N,N-dimethylformamide, the mixture was stirred for 10 minutes at room temperature. Boc-beta-ALA-OH (5.00 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (7.59 g) and 1-hydroxybenzotriazole (5.35 g) were added thereto, and the mixture was stirred at room temperature for 3 days. The reaction mixture was partitioned between ethyl acetate and brine. The organic layer was washed with brine and dried over anhydrous sodium sulfate. It was then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent; ethyl acetate, then ethyl acetate:methanol=10:1). Fractions containing the target compound were concentrated under reduced pressure to provide the title compound (5.99 g, 99.4%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531532B2
Source datasetuspto-grants-2009_05
ORD IDord-9ca49354934640d08ddcc414b7de6308
Source noteuspto-grants-2009_05