HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → HCID 15288740, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 2-Pyridineethanamine | HCID 75919 | — |
| Reactant | 2-[[(8-chlorodibenz[b,f][1,4]oxazepin-10(11H)-yl)carbonyl]amino]acetic acid | HCID 10830447 | — |
| Product | HCID 15288740 | HCID 15288740 | 55.2% |
Reaction Steps
By the method described in Example 5, the title compound of Example 4 (0.5 g, 1.5 mmol) in 20 mL of CH2CL2 was converted to its mixed anhydride with NMM (0.16 mL, 1.5 mmol) and IBCF (0.2 mL, 1.5 mmol) and coupled to 2-(2-aminoethyl)pyridine (0.18 mL, 1.5 mmol). This procedure gave 362 mg of the title compound after Chromatotron® chromatography eluting with 5% ethanol (EtOH)/CH2CL2 containing 1% ammonium hydroxide (NH4OH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05441950 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-035e8d27ab39419494a451226a80d706 |
| Source note | uspto-grants-1995_08 |