HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acryloyl chloride → HCID 178460028, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | HCID 178460971 | HCID 178460971 | — |
| Reactant | N-[2-hydroxy-4-[[[(Z)-(6-iodo-1,3-dioxoisoquinolin-4-ylidene)methyl]amino]methyl]phenyl]benzamide | HCID 178518369 | — |
| Product | HCID 178460028 | HCID 178460028 | — |
Reaction Steps
Following the acetylation and desilylation procedure employed for the preparation of N-[2-hydroxy-4-({[(Z)-(6-iodo-1,3-dioxo-2,3-dihydroisoquinolin-4(1H)-ylidene)methyl]amino}methyl)phenyl]benzamide, (4Z)-4-[({4-amino-3-[(triisopropylsilyl)oxy]benzyl}-amino)methylene]-6-bromoisoquinoline-1,3(2H,4H)-dione (54 mg, 0.10 mmol) is reacted with acryloyl chloride (41 μL, 0.50 mmol). Following desilylation, precipitation, and washing with methanol and diethyl ether, N-[4-({[(Z)-(6-bromo-1,3-dioxo-2,3-dihydroisoquinolin-4(1H)-ylidene)methyl]amino}methyl)-2-hydroxyphenyl]acrylamide is obtained (8 mg, 18
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713994B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-d42724c20c8f4ff99a0abc2c5998d37f |
| Source note | uspto-grants-2010_05 |