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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603452Generated: November 1, 2026

allyl (1S,5R,6S)-2-(hydroxymethyl)-6-[1(R)-allyloxycarbonyloxy-ethyl]-1-methylcarbapen-2-em-3-carboxylate → (1S,5R,6S)-6-[(1R)-1-hydroxyethyl]-2-(2-(formylamino)methyl-3-methylimidazo[5,1-b]thiazolium-6-yl)methyl-1-methyl-1-carbapen-2-em-3-carboxylate

https://huagongshe.com/reaction/1603452

Reaction equation

Participants

RoleNameHCIDCharge
Reactantallyl (1S,5R,6S)-2-(hydroxymethyl)-6-[1(R)-allyloxycarbonyloxy-ethyl]-1-methylcarbapen-2-em-3-carboxylateHCID 11046746—
Reactant2-(Formylamino)methyl-3-methylimidazo[5,1-b]thiazoleHCID 19605013—
Product(1S,5R,6S)-6-[(1R)-1-hydroxyethyl]-2-(2-(formylamino)methyl-3-methylimidazo[5,1-b]thiazolium-6-yl)methyl-1-methyl-1-carbapen-2-em-3-carboxylateHCID 1784286853.8%

Reaction Steps

The same procedure as in Example 1 was repeated except that 91.3 mg of allyl (1S,5R,6S)-6-[(1R)-1-allyloxycarbonyloxyethyl]-2-hydroxymethyl-1-methyl-1-carbapen-2-em-3-carboxylate and 100 mg of 2-(formylamino)methyl-3-methylimidazo[5,1-b]thiazole were used, thereby obtaining 4 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990101
Source datasetuspto-grants-1999_11
ORD IDord-4a404029b9bd4005ba11a8498e7a5cdf
Source noteuspto-grants-1999_11