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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763472Generated: October 30, 2026

tert-Butyl N,N-dipropan-2-ylcarbamimidate → HCID 178468125, compound

https://huagongshe.com/reaction/1763472

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl N,N-dipropan-2-ylcarbamimidateHCID 22010542—
ReactantHCID 178468132HCID 178468132—
SolventDichloromethaneHCID 6344—
ProductHCID 178468125HCID 178468125—

Reaction Steps

To a suspension of 21.8 g (0.05 mol) of 7β-amino-3-(1-ethoxyhydroxyphosphinylmethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid in 500 ml of methylene chloride is added over a 30 minute interval a solution of 60.0 g (0.30 mol) of O-t-butyldiisopropylpseudourea in 100 ml of methylene chloride. The mixture is stirred at ambient temperature for 72 hours. The precipitate is removed by filtration and the filtrate is evaporated to a residue which is taken up in 200 ml of benzene and filtered again. The filtrate is extracted with three 100 ml portions of cold 1N hydrochloric acid. The aqueous extracts are layered with ethyl acetate and the pH is adjusted to 7.5 by addition of solid sodium bicarbonate. The organic layer is separated and the aqueous phase is extracted with two 150 ml portions of ethyl acetate. The combined extracts are dried (MgSO4), filtered and evaporated to dryness to give 7β-amino-3-(1-ethoxy-t-butoxyphosphinylmethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid t-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04112086
Source datasetuspto-grants-1978_09
ORD IDord-93af2282ebeb444d8b07e1077e2c9208
Source noteuspto-grants-1978_09