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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418172Generated: November 2, 2026

Hydrochloric Acid → HCID 86736761, compound

https://huagongshe.com/reaction/2418172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86736762HCID 86736762—
SolventMethanolHCID 887—
ProductHCID 86736761HCID 8673676174.7%

Reaction Steps

2-[3-{4-(3-tert-butoxycarbonylamino-3-methoxycarbonylpropoxy) phenylglyoxyloylamino}-2-oxo-1-azetidinyl]-2-(2-thienyl)acetic acid (0.480 g.) was dissolved in methanol (3 ml.), and to the solution, there was added 1N aqueous sodium hydroxide (2 ml.) under ice-cooling. The mixture was stirred at the same temperature for 7 hours while adjusting to pH 9.0 to 9.5 with 1N aqueous sodium hydroxide. After the reaction, the reaction mixture was adjusted to pH 7.0 with dilute hydrochloric acid and evaporated to dryness under reduced pressure on a water bath. The resultant residue was dissolved in a small amount of water, and the aqueous solution was adjusted to pH 5.5 with dilute hydrochloric acid and then washed with ethyl acetate. The aqueous solution was adjusted to pH 4.0 to 4.5 with dilute hydrochloric acid and then extracted with ethyl acetate. This extract was evaporated to dryness under reduced pressure to give 2-[3-{4-(3-tert-butoxycarbonylamino-3-carboxypropoxy) phenylglyoxyloylamino}-2-oxo-1 -azetidinyl]-2-(2-thienyl) acetic acid (0.350 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04472309
Source datasetuspto-grants-1984_09
ORD IDord-12cf16c5632746ff8c4ac0ef21308f26
Source noteuspto-grants-1984_09