HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylethanolamine → HCID 16039137, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylethanolamine | HCID 1000 | — |
| Reactant | 2,2,2-Trichloro-1-{10-[(2-methoxy-2'-methyl-1,1'-biphenyl-4-yl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-3-yl}ethanone | HCID 16038825 | — |
| Product | HCID 16039137 | HCID 16039137 | — |
Reaction Steps
The title compound was prepared in the manner of Example 36 from 2,2,2-trichloro-1-{10-[(2-methoxy-2′-methyl-1,1′-biphenyl-4-yl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-3-yl}ethanone of Example 35 and (±)-2-amino-1-phenylethanol. Purification was performed using HPLC with a normal phase column. Elution with a two phase solvent system (A=hexane, B=dichloromethane/methanol, 4:1) gave the title compound in 77% yield, m.p. 214-215° C. MS [(+)ESI, m/z]: 572 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691848B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-f8074e3d3e9040c6845ef9d75a0c71b7 |
| Source note | uspto-grants-2010_04 |