HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenothiazine → HCID 486243, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenothiazine | HCID 7108 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-[(N-phenylanilino)methyl]pteridine-2,4-diamine | HCID 486242 | — |
| Reactant | 6-(Bromomethyl)-2-imino-2,3-dihydropteridin-4-amine--hydrogen bromide (1/1) | HCID 12503242 | — |
| Product | HCID 486243 | HCID 486243 | — |
Reaction Steps
N-[(2,4-Diaminopteridin-6-yl)methyl]phenothiazine (Formula I: Ar=2,4-diaminopteridin-6-yl; W=CH2 X=N; Z=S; m=n=0) is prepared similarly to N-[(2,4-diaminopteridin-6-yl)methyl]-N,N-diphenylamine as disclosed above by using phenothiazine (159 mg, 0.8 mmol), NaH (50 mg, 2.1 mmol), and 2,4-diamino-6-bromomethylpteridine hydrobromide (100 mg, 0.3 mmol). The product can be purified by chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07056911B1 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-006da8ad07b54718b2adf56a34198191 |
| Source note | uspto-grants-2006_06 |