HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenothiazine → 9-[(2,4-Diaminofuro[2,3-d]pyrimidin-5-yl)methyl]phenothiazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenothiazine | HCID 7108 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | n-[(2,4-Diaminofuro[2,3-d]pyrimidin-5-yl)methyl]-n,n-diphenylamine | HCID 9818937 | — |
| Reactant | 5-(Chloromethyl)furo[2,3-d]pyrimidine-2,4-diamine | HCID 11412959 | — |
| Product | 9-[(2,4-Diaminofuro[2,3-d]pyrimidin-5-yl)methyl]phenothiazine | HCID 22062980 | — |
Reaction Steps
9-[(2,4-Diaminofuro[2,3-d]pyrimidin-5-yl)methyl]phenothiazine (Formula I: Ar=2,4-diaminofuro[2,3-d]pyrimidin-5-yl; W=CH2; X=N; Z=S; m=n=0) is prepared similarly to N-[(2,4-diaminofuro[2,3-d]pyrimidin-5-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-5-chloromethylfuro[2,3-d]pyrimidine (60 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-75a372aab9214ff0a3a9ac9ee10b4b18 |
| Source note | uspto-grants-2006_06 |