HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → Hydrochloric Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 3-Bromobenzyl bromide | HCID 69979 | — |
| Reactant | HCID 66826663 | HCID 66826663 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 66826663 | HCID 66826663 | — |
Reaction Steps
In a similar manner N-(3-((((4R,4aS,6R,7R,7aR,12bS)-3-(cyclopropylmethyl)-9-hydroxy-7-methoxy-1,2,3,4,5,6,7,7a-octahydro-4a,7-ethano-4,12-methanobenzofuro[3,2-e]isoquinolin-6-yl)methoxy)methyl)phenyl)acetamide (Compound 72) was prepared from R-101 using 3-bromobenzyl bromide, followed by conversion of the aryl bromide to the aniline, subsequent reaction of the aniline with acetyl chloride and final cleavage of the p-methoxybenzyl group by TFA. Purification by flash column chromatography (silica gel, 0-10% MeOH/DCM) followed by HCl salt formation gave Compound 72 HCl salt as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221831B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-0941c1880ace4f5facd328eec2ab4b70 |
| Source note | uspto-grants-2015_12 |