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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653268Generated: October 29, 2026

HCID 86740397, compound → HCID 86740418, compound

https://huagongshe.com/reaction/653268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86740397HCID 86740397—
ReactantHCID 86740419HCID 86740419—
SolventMethanolHCID 887—
ProductHCID 86740418HCID 8674041841.4%

Reaction Steps

To a solution of 0.260 g of the above sodium (3R,4R)-3-[2-(2-chloroacetamidothiazol-4-yl)-2-methoxyiminoacetamido]-4-(1-methyl-1H-tetrazol-5-yl)thio-2-oxoazetidine-1-sulfonate in 20 ml of 50% methanol is added under ice-cooling 0.0597 g of sodium monomethyldithiocarbamate, and the mixture is stirred at room temperature for 5 hours. The same procedure as Example 3B yields 0.093 g of sodium (3R,4R)-3-[2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-4-(1-methyl-1H-tetrazol-5-yl)thio-2-oxoazetidine-1-sulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04675397
Source datasetuspto-grants-1987_06
ORD IDord-712d54b194c144fa9f86e8fb8b92fc97
Source noteuspto-grants-1987_06