HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloro-4-methoxybenzylamine → HCID 15871163, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloro-4-methoxybenzylamine | HCID 738038 | — |
| Reactant | HCID 15871166 | HCID 15871166 | — |
| Reactant | HCID 86587249 | HCID 86587249 | — |
| Reactant | HCID 178527823 | HCID 178527823 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 15871163 | HCID 15871163 | 125.5% |
Reaction Steps
A mixture of 1.5 g of methyl 4-(4-chlorobenzothieno[2, 3-d]pyrimidin-2-yl)phenylcarboxylate (“B”), prepared by dehydrogenation of the corresponding 5,6,7,8-tetrahydrobenzothieno[2,3-d]pyrimidine compound with sulfur and subsequent chlorination with phosphorus oxychloride/dimethylamine, and 1.5 g of 3-chloro-4-methoxybenzylamine in 20 ml of N-methylpyrrolidone is heated at 110° for 4 hours. After cooling, the mixture is worked up in the customary manner. 2.6 g of methyl 4-[4-(3-chloro-4-methoxybenzylamino)benzothieno[2,3-d]pyrimidin-2-yl]-benzoate, m.p. 203-204°, are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06787548B1 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-b395470e5de149769e967ef164341fd8 |
| Source note | uspto-grants-2004_09 |