HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 70117622, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 10117643 | HCID 10117643 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70117622 | HCID 70117622 | — |
Reaction Steps
A solution of 0.02 g (0.04 mmol) of 1-(2,4-dichlorobenzyl)-3-(S)-(4-(3-hydroxypropyloxymethyl)piperidinylmethyl)-4-(S)-(3-thienyl)pyrrolidine (Example 17), 0.25 mL (0.12 mmol) of acetic anhydride, 0.25 mL (0.3 mmol) of pyridine and a catalytic amount of DMAP in 0.5 mL of CH2Cl2 was stirred at rt for 2 h. TO the reaction mixture was added 10 mL of sat'd Na2CO3 solution and it was extracted with CH2Cl2. The combined organic layers were dried over MgSO4, filtered and the filtrate was concentrated. The residue was purified by chromatography (silica, hexanes:ethyl acetate, 1:1) to give the title compound. Mass Spectrum (ESI) m/e=539 (M+1 35Cl, 35Cl), 541 (M+1 35Cl, 37Cl), and 543 (M+1 37Cl, 37Cl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06455548B2 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-bf015af8e8f049b59d21e4b8cc6ce050 |
| Source note | uspto-grants-2002_09 |