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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2087120Generated: October 26, 2026

Methanol → HCID 22672527, compound

https://huagongshe.com/reaction/2087120

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 numberUS06727356B1
Source datasetuspto-grants-2004_04
ORD IDord-d8f5711b417e439cb3ed1e47350ec1e0
Source noteuspto-grants-2004_04