HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Methylhydroxylamine → N-Benzyloxy-3-(2-chloro-4-iodo-phenylamino)-isonicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Methylhydroxylamine | HCID 4113 | — |
| Reactant | 3-[(2-Chloro-4-iodophenyl)amino]isonicotinic acid | HCID 57649651 | — |
| Product | N-Benzyloxy-3-(2-chloro-4-iodo-phenylamino)-isonicotinamide | HCID 11677348 | — |
Reaction Steps
N-Benzyloxy-3-(2-chloro-4-iodo-phenylamino)-isonicotinamide was synthesized according to the procedure for General Method 1, outlined above, starting with 0.25 mmol of 3-[(2-chloro-4-iodophenyl)amino]isonicotinic acid (intermediate 2) and 0.36 mmol of O-methyl-hydroxylamine. LC/MS [10.0]min; 480 (M+1)]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07956191B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-23e2fbf1e4a34036937ad47e0b3646d7 |
| Source note | uspto-grants-2011_06 |