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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47969Generated: October 25, 2026

Methanol → HCID 22672527, compound

https://huagongshe.com/reaction/47969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
Reactant2-Cyanoethyl N,N-diisopropylchlorophosphoramiditeHCID 2734844—
Reactant8-(3-Hydroxypropyl)-7-oxophenoxazin-3-yl 2,2-dimethylpropanoateHCID 22672525—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductHCID 22672527HCID 22672527—

Reaction Steps

36b (0.38 g, 1.1 mmol) was dissolved in 6 mL of anhydrous CH2Cl2. Triethylamine (1.5 mL) was added followed by 2-cyanoethyl diisopropylchlorophosphoramidite (0.29 mL, 1.3 mmol). The solution was kept at room temperature for 30 min, MeOH (0.1 mL) was added and the reaction was concentrated under vacuum. The residue obtained was partitioned between ethyl acetate and NaHCO3. The organic phase was washed with saturated NaCl, dried over Na2SO4 and concentrated to afford the crude amidite. It was dissolved in 2 mL of ether and added dropwise to ˜50 mL of hexane. The resultant orange solid was collected by filtration, washed with hexane and dried. The yield was 0.4 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699975B2
Source datasetuspto-grants-2004_03
ORD IDord-12f83a610c1f470193d59c21eab882af
Source noteuspto-grants-2004_03