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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704513Generated: October 29, 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/704513

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(hydroxymethyl)-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 crystallize, 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 numberUS04987129
Source datasetuspto-grants-1991_01
ORD IDord-c342f50b6ccd41e3a04800d7e5f46d2d
Source noteuspto-grants-1991_01