HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 454704, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Tetradecanoic anhydride | HCID 69377 | — |
| Reactant | N-(9-Fluorenylmethoxycarbonyloxy)succinimide | HCID 134122 | — |
| Reactant | HCID 454703 | HCID 454703 | — |
| Reactant | 1,2-Bis(12-methoxydodecanoyl)-sn-glycero-3-phosphocholine | HCID 3081311 | — |
| Product | HCID 454704 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05846955 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-7e6850bc84e94e198961b7a505b55449 |
| Source note | uspto-grants-1998_12 |