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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005938Generated: October 31, 2026

3-Chloro-4-methoxybenzylamine → HCID 15871163, compound

https://huagongshe.com/reaction/1005938

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-methoxybenzylamineHCID 738038—
ReactantHCID 15871166HCID 15871166—
ReactantHCID 86587249HCID 86587249—
ReactantHCID 178527823HCID 178527823—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 15871163HCID 15871163125.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787548B1
Source datasetuspto-grants-2004_09
ORD IDord-b395470e5de149769e967ef164341fd8
Source noteuspto-grants-2004_09