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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456923Generated: October 30, 2026

Piperidine → HCID 454704, compound

https://huagongshe.com/reaction/1456923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTetradecanoic anhydrideHCID 69377—
ReactantN-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
ReactantHCID 454703HCID 454703—
Reactant1,2-Bis(12-methoxydodecanoyl)-sn-glycero-3-phosphocholineHCID 3081311—
ProductHCID 454704HCID 454704—

Reaction Steps

The preparation of D-AC2 was identical to L-AC2 except D-glycerolphosphocholine, which was obtained from Synthetische Phosphor-Lipide, Biochemisches Labor, Bern CH Switzerland was used. L-PE2 was prepared by reacting glycerolphosphatidylethanolamine (L-a-GPE) with N-(9-Fluorenylmethoxycarbonyloxy) succinimide (FMOC-succinimide) to form L-a-GPE-FMOC followed by diacylation with 12MO anhydride then deprotection of FMOC with piperidine. L-PE1 was prepared by diacylating L-a-GPE-FMOC with myristic anhydride, then PLA2 cleavage to remove the sn-2 chain, then acylation with 12MO anhydride, and finally deprotection with piperidine to remove FMOC. ##STR47##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05846955
Source datasetuspto-grants-1998_12
ORD IDord-7e6850bc84e94e198961b7a505b55449
Source noteuspto-grants-1998_12