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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375767Generated: October 30, 2026

Pyridine → HCID 53913232, compound

https://huagongshe.com/reaction/375767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 53751378HCID 53751378—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 53913232HCID 5391323239.1%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 25 mg of the product of Example 159 and 0.1 ml of pyridine in 1.5 ml of acetic anhydride was stirred at 20° C. for 3 hours. The precipitate was collected by filtration, washed with pentane, and dissolved in 1.5 ml of methanol. After the addition of 2.6 mg of potassium carbonate, the mixture was stirred for 1.5 hours at 20° C., and then evaporated in vacuo. Water was added to the residue, and the insoluble material was isolated by filtration, to yield 7 mg of tert-butyl (4R,7S)-12-acetylamino-1,3,4,5,6,7,8,10-octahydro-14-hydroxy-4-methoxycarbonyl-6,10-dioxo-9,2,5-benzoxathiaazacyclododecine-7-carbamate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05486466
Source datasetuspto-grants-1996_01
ORD IDord-3f80976e62ba4e6bb1a65c5ab68b348a
Source noteuspto-grants-1996_01