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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919361Generated: November 1, 2026

Tert-butyl octahydropyrrolo(3,4-c)pyrrole-2-carboxylate → 5-(5-Chloro-7-morpholin-4-yl-thiazolo[4,5-d]pyrimidin-2-ylmethyl)-hexahydro-pyrrolo[3,4-c]pyrrole-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1919361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl octahydropyrrolo(3,4-c)pyrrole-2-carboxylateHCID 4142526—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-Chloro-7-morpholinothiazolo[4,5-d]pyrimidine-2-carbaldehydeHCID 57685392—
Solvent1,2-DichloroethaneHCID 11—
Product5-(5-Chloro-7-morpholin-4-yl-thiazolo[4,5-d]pyrimidin-2-ylmethyl)-hexahydro-pyrrolo[3,4-c]pyrrole-2-carboxylic acid tert-butyl esterHCID 5823493761.4%

Reaction Steps

To a solution of 5-chloro-7-morpholin-4-yl-thiazolo[4,5-d]pyrimidine-2-carbaldehyde (25 mg, 0.088 mmol) in 1,2-dichloroethane (1 mL) was added hexahydro-pyrrolo[3,4-c]pyrrole-2-carboxylic acid tert-butyl ester (21 mg, 0.10 mmol). The mixture was stirred at RT for 5 min before sodium triacetoxyborohydride (28 mg, 0.130 mmol) was added. The resulting solution was stirred at RT for 1 h. The crude reaction mixture was partitioned between DCM and brine. The organic layer was isolated, then dried (MgSO4) and concentrated in vacuo. The resultant residue was purified by column chromatography to give the title compound as a white solid (26 mg, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168633B2
Source datasetuspto-grants-2012_05
ORD IDord-2bb097c172284fde867007b33987286d
Source noteuspto-grants-2012_05