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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422178Generated: October 29, 2026

4-Methylmorpholine → HCID 53240853, compound

https://huagongshe.com/reaction/422178

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantMorpholineHCID 8083—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 53240650HCID 53240650—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53240853HCID 5324085352.6%

Reaction Steps

A mixture of (1R,10R,11S,16S)-5-hydroxy-1,11,15,15-tetramethyl-8,8-dioxo-8λ6-thiatetracyclo[8.8.0.02,7.011,16]octadeca-2,4,6-triene-3-carboxylic acid (65) (0.06 g, 0.2 mmol), HATU (0.15 g, 0.40 mmol), N-methylmorpholine (0.04 mL, 0.6 mmol) and morpholine (0.1 mL, 1 mmol) in THF (4.0 mL) and DMF (1.0 mL) was stirred at room temperature for 18 h. The THF was evaporated under reduced pressure, the residue was quenched with water and the resulting solid was collected by filtration. The crude product was purified by flash column chromatography on silica gel (Hexanes/EtOAc, 3:1) to give (1R,10R,11S,16S)-5-hydroxy-1,11,15,15-tetramethyl-3-[(morpholin-4-yl)carbonyl]-8λ6-thiatetracyclo-[8.8.0.02,7.011,16]octadeca-2,4,6-triene-8,8-dione (88) (0.05 g, 45%) as a tan solid. 1H NMR (DMSO-d6): δ 8.49 (s, 1H), 7.14 (s, 1H), 6.75 (s, 1H), 3.72-3.14 (m, 10H), 2.44 (m, 1H), 2.00 (d, 1H), 1.83 (d, 1H), 1.70-1.32 (m, 8H), 1.28-1.22 (m, 1H), 1.12 (m, 1H), 0.96 (m, 1H), 0.89 (s, 3H), 0.86 (m, 3H), 0.82 (m, 1H), 0.79 (s, 3H). MS m/z 476 (C26H37NO6S+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101605B2
Source datasetuspto-grants-2012_01
ORD IDord-fb07f0aefc0848858c9feb224900b318
Source noteuspto-grants-2012_01