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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27143Generated: October 30, 2026

tert-Butyl N,N-dipropan-2-ylcarbamimidate → HCID 178450678, compound

https://huagongshe.com/reaction/27143

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl N,N-dipropan-2-ylcarbamimidateHCID 22010542—
Reactant7-Amino-3-[1-(2-carbamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acidHCID 178513909—
SolventDichloromethaneHCID 6344—
ProductHCID 178450678HCID 178450678—

Reaction Steps

To a suspension of 19.3 g. (0.05 mol.) of 7-amino-3-[1-(2-carbamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid in 500 ml. of dry methylene chloride is added in one portion 30.0 g. (0.15 mol.) of O-t-butyldiisopropylpseudourea in 50 ml. of methylene chloride and the mixture is stirred at ambient temperature for 24 hours. The precipitate is removed by filtration and the filtrate is evaporated to give 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 7-amino-3-[1-(2-carbamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid t-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04220644
Source datasetuspto-grants-1980_09
ORD IDord-f11b8c37a12540549fe51ebc977465c0
Source noteuspto-grants-1980_09