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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032595Generated: October 31, 2026

Methanol → Diphenylmethyl 7-amino-3-[(2,5-bis(hydroxymethyl)-s-triazolo[1,5-a]pyrimidin-7-yl)thiomethyl]-3-cephem-4-carboxylate

https://huagongshe.com/reaction/1032595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1,1'-(Diazomethylene)bis(benzene)HCID 61230—
ReactantDiphenylmethylidenehydrazineHCID 79304—
Reactant7-Amino-3-[(2,5-bis(hydroxy-methyl)-s-triazolo[1,5-a]pyrimidin-7-yl)thiomethyl]-3-cephem-4-carboxylic acidHCID 131716552—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductDiphenylmethyl 7-amino-3-[(2,5-bis(hydroxymethyl)-s-triazolo[1,5-a]pyrimidin-7-yl)thiomethyl]-3-cephem-4-carboxylateHCID 131716553—

Reaction Steps

In a suspension of 5.3 g of 7-amino-3-[(2,5-bis(hydroxy- methyl)-s-triazolo[1,5-a]pyrimidin-7-yl)thiomethyl]-3-cephem-4-carboxylic acid, 35 ml of methanol and 100 ml of methylene chloride was added dropwise, while stirring, diphenyldiazomethane synthesized from 6.9 g of benzophenonehydrazone, 7.6 g of mercuric oxide (yellow) and 70 ml of n-hexane, in 30 ml of methylene chloride solution, and the mixture was stirred at room temperature overnight. After the reaction mixture was condensed, ether was added thereto to crystalize, and crystal was collected by filtration and dried to obtain 7.28 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04958019
Source datasetuspto-grants-1990_09
ORD IDord-7f6bfd0a09d341459903de2fa1bb0f4a
Source noteuspto-grants-1990_09