HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 9964396, compound → N-Decylprop-2-enimidic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 9964396 | HCID 9964396 | — |
| Reactant | HCID 11126788 | HCID 11126788 | — |
| Reactant | HCID 21258221 | HCID 21258221 | — |
| Product | N-Decylprop-2-enimidic acid | HCID 3018705 | — |
Reaction Steps
The same procedure as in Example 18 was repeated except that N-(4-phenylbutyl)acrylamide, N-(10-phenyldecyl)acrylamide and N-phenethylacrylamide were used, respectively, in place of N-decylacrylamide to obtain N-cyclopropylmethyl-7α-(4-phenylbutylcarbamoyl)-6,14-endoethenotetrahydronormorphide 25.methanesulfonic acid salt (39%), N-cyclopropylmethyl-7β-(4-phenylbutylcarbamoyl)-6,14-endoethenotetrahydronormorphide 26.methanesulfonic acid salt (5%), N-cyclopropylmethyl-7α-(10-phenyldecylcarbamoyl)-6,14-endoethenotetrahydronormorphide 27.methanesulfonic acid salt (21%), and N-cyclopropylmethyl-7β-phenethylcarbamoyl-6,14-endoethenotetrahydronormorphide 28.methanesulfonic acid salt (3%), respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06187782B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-5aae70bdb4d24318b7dee0fc637ff2fa |
| Source note | uspto-grants-2001_02 |