HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → HCID 16105853, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | HCID 5335896 | HCID 5335896 | — |
| Reactant | HCID 16105853 | HCID 16105853 | — |
| Product | HCID 16105853 | HCID 16105853 | — |
| Product | HCID 59656326 | HCID 59656326 | — |
Reaction Steps
4-[4-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-naphthalene-1-sulfonylamino]-piperidine-1-carboxylic acid tert-butyl ester (19) was prepared according to the general procedure in Scheme 3, substituting 4-amino-piperidine-1-carboxylic acid tert-butyl ester for p-anisidine. 4-(4-Amino-naphthalene-1-sulfonylamino)-piperidine-1-carboxylic acid tert-butyl ester (20) was prepared according to the general procedure in Scheme 3 substituting 4-[4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-naphthalene-1-sulfonylamino]-piperidine-1-carboxylic acid tert-butyl ester for 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-naphthalene-1-sulfonic acid (4-methoxyphenyl)-amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07329755B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-121860fefb364986aba3314d07f9cc54 |
| Source note | uspto-grants-2008_02 |