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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169558Generated: October 31, 2026

Sodium t-butoxide → HCID 86670106, compound

https://huagongshe.com/reaction/2169558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium t-butoxideHCID 23676156—
Reactant2-(Chloromethyl)-5-cyclopropyl-1,3,4-oxadiazoleHCID 28063957—
ReactantHCID 86670087HCID 86670087—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 86670106HCID 86670106—

Reaction Steps

The title compound was prepared in a manner similar to PREPARATION x9 using 2-chloro-5,6,6a,7,9,10-hexahydro-[1,4]oxazino[3,4-h]pteridine (PREPARATION x2, 75 mg, 0.331 mmol) in DMSO (2 mL) followed by sodium tert-butoxide (35.0 mg, 0.364 mmol) and 2-(chloromethyl)-5-cyclopropyl-1,3,4-oxadiazole (68.2 mg, 0.430 mmol). 1H NMR (400 MHz, DMSO-d6) δ 0.92-1.00 (m, 2 H), 1.07-1.16 (m, 2 H), 2.14-2.25 (m, 1 H), 2.92-3.03 (m, 1 H), 3.03-3.11 (m, 1 H), 3.11-3.20 (m, 1 H), 3.34-3.51 (m, 1 H), 3.53-3.58 (m, 1 H), 3.59-3.72 (m, 1 H), 3.85-4.00 (m, 2 H), 4.20-4.29 (m, 1 H), 4.53-4.63 (m, 1 H), 4.79-4.88 (m, 1 H), 7.56 (s, 1 H). ESI-MS m/z [M+H]+ calc'd for C15H17ClN6O2, 348.11; found 348.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045496B2
Source datasetuspto-grants-2015_06
ORD IDord-2285723f26ec477fae31c6c6ce6a932c
Source noteuspto-grants-2015_06