HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178431207, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | MAGNESIUM SILICATE (synthetic) | HCID 61680 | — |
| Reactant | (E)-6-bromo-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione | HCID 68692760 | — |
| Reactant | HCID 68699088 | HCID 68699088 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178431207 | HCID 178431207 | — |
Reaction Steps
(4E)-6-bromo-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione (0.42 g, 1.5 mmol) and C-(7-benzyloxy-2,2-dimethyl-benzo[1,3]dioxol-5-yl)-methylamine hydrochloride (1.5 mmol) were coupled in N,N-dimethylformamide (10 mL) with triethylamine (0.6 mL). The crude material is dissolved in a minimum of 7.5% methanol in chloroform and then passed through a Florisil plug, eluting with 5% methanol in chloroform. The filtrate is concentrated under reduced pressure to give (4Z)-6-bromo-4-({[(7-hydroxy-2,2-dimethyl-1,3-benzodioxol-5-yl)methyl]amino}methylene)isoquinoline-1,3(2H,4H)-dione as a light pink powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713994B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-6fdd613f376b4d3a978dde764b3dfd14 |
| Source note | uspto-grants-2010_05 |