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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729567Generated: October 27, 2026

Morpholine → HCID 141573540, compound

https://huagongshe.com/reaction/1729567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant(Oxan-4-yl)methanolHCID 2773573—
ReactantTetrahydropyran-4-ylmethyl trifluoromethanesulfonateHCID 19011570—
ReactantHCID 141559367HCID 141559367—
SolventPyridineHCID 1049—
SolventTriethylamineHCID 8471—
ProductTetrahydropyran-4-ylmethyl trifluoromethanesulfonateHCID 19011570—
ProductHCID 141573540HCID 14157354098%

Reaction Steps

Tetrahydropyran-4-ylmethyl trifluoromethanesulfonate was prepared in the same manner as in Example 27 (a) from tetrahydropyran-4-yl-methanol (223 mg), pyridine (0.17 ml) and trifluoromethanesulfonic acid anhydride (596 mg). On the other hand, diphenylmethyl 7-[(Z)-2-(2-tritylaminothiazol-4 -yl) -2 -trityloxyiminoacetamido]-3-acetylthio-3-cephem-4-carboxylate (700 mg) was reacted with morpholine and triethylamine in the same manner as in Example 27(b), followed by reacting the resulting reaction product with the tetrahydropyran-4-ylmethyl trifluoromethanesulfonate in the same manner as in Example 27 (b).The reaction solution so obtained was post-treated in the same manner as in Example 27 (b) and the produced compound was recovered and purified similarly to Example 27 (b) to afford the titled compound (722 mg; 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05332731
Source datasetuspto-grants-1994_07
ORD IDord-b18fe417a76e4582b78d4bc27bceb4bd
Source noteuspto-grants-1994_07