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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242307Generated: October 31, 2026

tert-Butyl (3S)-3-hydroxypyrrolidine-1-carboxylate → (S)-3-(6-Benzyl-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-yloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/242307

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (3S)-3-hydroxypyrrolidine-1-carboxylateHCID 854055—
Reactant6-Benzyl-4-chloro-5,6,7,8-tetrahydropyrido(4,3-d)pyrimidineHCID 25324046—
Product(S)-3-(6-Benzyl-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-yloxy)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 5749530292.6%

Reaction Steps

To a solution of (S)-3-hydroxypyrrolidine-1-carboxylic acid tert-butyl ester (6.21 g, 33.16 mmol) and 6-benzyl-4-chloro-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidine (9 g, 34.65 mmol) in 2-Me-THF (100 mL) was added under nitrogen tBuOK (8.17 g, 72.95 mmol). The mixture was stirred at rt for 25 min. The mixture was quenched with H2O. The organic layer was washed with brine. The resulting organic solution was concentrated in vacuo to provide (S)-3-(6-benzyl-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-4-yloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester (12.6 g, 89% yield) as a yellow gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653092B2
Source datasetuspto-grants-2014_02
ORD IDord-aa5f26f85e2e42d4b89786180e5e4bfb
Source noteuspto-grants-2014_02