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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626539Generated: October 29, 2026

(S)-tert-butyl 2-chloro-4-(3-methylmorpholino)-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylate → (S)-4-(2-chloro-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-4-yl)-3-methylmorpholine hydrochloride

https://huagongshe.com/reaction/1626539

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-tert-butyl 2-chloro-4-(3-methylmorpholino)-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylateHCID 86663148—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Product(S)-4-(2-chloro-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-4-yl)-3-methylmorpholine hydrochlorideHCID 86663150—

Reaction Steps

A solution of (S)-tert-butyl 2-chloro-4-(3-methylmorpholino)-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylate (intermediate 1) (200 mg, 0.56 mmol) in 1M HCl in EtOH (5 mL) was stirred at room temperature (20° C.) overnight. The material was concentrated in vacuo to give a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785457B2
Source datasetuspto-grants-2014_07
ORD IDord-86c45b17f69b4a57a34bdfe7fd5a1fac
Source noteuspto-grants-2014_07