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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474159Generated: October 29, 2026

Diisopropylethylamine → [1-(2-Chloro-6,7-dihydrothieno[3,2-d]pyrimidin-4-ylamino)-cyclopropyl]-methanol

https://huagongshe.com/reaction/474159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(1-Aminocyclopropyl)methanolHCID 14146220—
Reactant2,4-Dichloro-6,7-dihydrothieno[3,2-d]pyrimidineHCID 45789967—
Solvent1,4-DioxaneHCID 31275—
Product[1-(2-Chloro-6,7-dihydrothieno[3,2-d]pyrimidin-4-ylamino)-cyclopropyl]-methanolHCID 59708441—

Reaction Conditions

Temperature160 °C

Reaction Steps

1.4 g (II) are placed in 10 ml dioxane, first 3.6 ml diisopropylethylamine, then 1 g of 1-aminocyclopropanemethanol (see 8.2) are added. The reaction mixture is heated to 160° C. until no further reaction takes place, then cooled and evaporated down. The residue is treated with cyclohexane/ethyl acetate (8:2) in the ultrasound bath and the solid is suction filtered and dried. 1.24 g (III-4) are obtained as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637519B2
Source datasetuspto-grants-2014_01
ORD IDord-de4c84c6b2f6424a865f00436f2c1f0d
Source noteuspto-grants-2014_01