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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169434Generated: October 31, 2026

Ethyl Acetate → HCID 178450821, compound

https://huagongshe.com/reaction/2169434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium MethoxideHCID 10942334—
Reactant(E)-2-benzyloxy-3-hydroxy-but-2-enedioic acid 4-tert-butyl esterHCID 86725882—
ReactantAcetic acid;2-(1-pyrrolo[2,3-b]pyridin-1-ylcyclopentyl)ethanimidamideHCID 86726064—
SolventMethanolHCID 887—
ProductHCID 178450821HCID 17845082175.4%

Reaction Steps

To a stirred solution of 2-(1-pyrrolo[2,3-b]pyridin-1-yl-cyclopentyl)-acetamidine; compound with acetic acid (402) (800 mg, 2.65 mmol) and (E)-3-benzyloxy-2-hydroxy-4-oxo-pent-2-enoic acid tert-butyl ester (4) (978 mg, 3.18 mmol) in methanol (80 mL) was added sodium methoxide solution (25% in methanol) (1.7 mL, 7.94 mmol) at 0° C. The reaction mixture was allowed to warm slowly to room temperature and was stirred for 16 h (TLC, ethyl acetate, Rf=0.3). After completion of the reaction, methanol was evaporated to get a crude product which was purified by Combi-Flash column (eluted at 60-70% ethyl acetate in hexane) to get 5-benzyloxy-6-hydroxy-2-(1-pyrrolo[2,3-b]pyridin-1-yl-cyclopentylmethyl)-pyrimidine-4-carboxylic acid tert-butyl ester (403) (1 g, 75%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045486B2
Source datasetuspto-grants-2015_06
ORD IDord-be57e476fb8a44d0b36bd91b73511355
Source noteuspto-grants-2015_06