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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403240Generated: November 2, 2026

Sodium hydride → 7H-Pyrrolo(2,3-d)pyrimidine

https://huagongshe.com/reaction/1403240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantTriisopropylsilyl chlorideHCID 139400—
Reactant7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
Reactant2-Chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 5706774—
SolventTetrahydrofuranHCID 8028—
Product7H-Pyrrolo(2,3-d)pyrimidineHCID 261591—

Reaction Steps

Compounds of Formula I or II, where P is a suitable protecting group, are prepared by reacting 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (1) or 2-chloro-7H-pyrrolo[2,3-d]pyrimidine (2), respectively, with an appropriate reagent to introduce a suitable protecting group (P—X, e.g. triisopropylsilylchloride) and a base (e.g. sodium hydride) in a solvent (e.g. tetrahydrofuran) typically at room temperature for 8-12 hours. The desired compound is isolated by conventional means (e.g. extraction).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912204B2
Source datasetuspto-grants-2014_12
ORD IDord-e9c041b2cddc4555b3fc112045ad7593
Source noteuspto-grants-2014_12