HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenothiazine → 9-[(2,4-Diaminothieno[2,3-d]pyrimidin-5-yl)methyl]phenothiazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenothiazine | HCID 7108 | — |
| Reactant | n-[(2,4-Diaminothieno[2,3-d]pyrimidin-5-yl)methyl]-n,n-diphenylamine | HCID 9906281 | — |
| Reactant | Thieno[2,3-d]pyrimidine-2,4-diamine, 5-methyl- | HCID 12659534 | — |
| Product | 9-[(2,4-Diaminothieno[2,3-d]pyrimidin-5-yl)methyl]phenothiazine | HCID 22063019 | — |
Reaction Steps
9-[(2,4-Diaminothieno[2,3-d]pyrimidin-5-yl)methyl]phenothiazine (Formula I: Ar=2,4-diaminothieno[2,3-d]pyrimidin-5-yl; W=CH2; X=N; Z=S; m=n=0) is prepared similarly to N-[(2,4-diaminothieno[2,3-d]pyrimidin-5-yl)methyl]-N,N-diphenylamine as disclosed in Example 11 above by using 2,4-diamino-5-methylthieno[2,3-d]pyrimidine (1.3 g, 7.4 mmol) in Step 1 and phenothiazine (159 mg, 0.8 mmol) in Step 3. The final product and its intermediates 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-fe20ee7f059d456c93876ee6f0635ffe |
| Source note | uspto-grants-2006_06 |