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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226597Generated: November 3, 2026

Diazomethane → HCID 53955469, compound

https://huagongshe.com/reaction/2226597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
ReactantHCID 22850672HCID 22850672—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 53955469HCID 53955469—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 368 mg (0.725 mmole) of (S)-4-(dipentylcarbamoyl)-1-(diphenylacetyl)piperazine-2carboxylic acid (from Example 9) in 5 ml of methanol was treated at 0° C. with 20 ml of diazomethane solution in diethyl ether (prepared by the procedure above). The solution was stirred at 0° C. for 30 minutes and at 25° C. for 30 minutes. The excess diazomethane was destroyed by the dropwise addition of acetic acid until the solution became colorless. The resulting solution was concentrated in vacuo and the residue was chromatographed over an 85×2.5 cm LH-20 column and concentrated in vacuo to 225 mg (59%) of pale colored oil which was homogeneous by TLC (1:1 hexane-ethyl acetate, Rf =0.7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05348955
Source datasetuspto-grants-1994_09
ORD IDord-54b74f756feb4e8faecfdc31c0b8fa72
Source noteuspto-grants-1994_09