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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533216Generated: October 29, 2026

Water → HCID 58158418, compound

https://huagongshe.com/reaction/533216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactantn-Butyl lithiumHCID 61028—
ReactantHCID 87240698HCID 87240698—
SolventDiethyl EtherHCID 3283—
SolventAnisoleHCID 7519—
ProductHCID 58158418HCID 5815841857.3%

Reaction Steps

7-Bromo-5-(benzyloxymethyl)-4-chloro-5H-pyrrolo[3,2-d]pyrimidine (3.73 g, 10.6 mmol) was dissolved in anhydrous anisole (48 ml) and then diluted with Et2O (145 ml) before being cooled to −78° C. at which point N-butyllithium (1.48M in hexane, 9.2 ml, 13.6 mmol) was added dropwise such that the temperature did not exceed −70° C. Within 2 minutes of the addition, DMF (8.5 ml, 0.123 mol) was introduced quickly (T≦−68° and the mixture stirred whilst warming to −40°, at which point water (20 ml) was added. The mixture was then extracted with EtOAc and the extract washed with brine and then dried and concentrated to an orange solid. Purification of this material was accomplished by chromatography over silica, eluting with 20→40% EtOAc/hexane, to give (a heart fraction of) the title aldehyde (1.83 g, 57.3%) as an off-white solid. 1H NMR (CDCl3) δ 10.35 (s, 1H), 8.89 (s, 1H), 8.14 (s, 1H), 7.35-7.20 (m, 5H), 5.90 (s, 2H), 4.60 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853224B2
Source datasetuspto-grants-2014_10
ORD IDord-163670c7c4ae473a8bff2ab0d22810a3
Source noteuspto-grants-2014_10