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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889880Generated: November 1, 2026

Methyl iodide → 7-chloro-2-[(R)-3-methoxypyrrolidine-1-carbonyl]thieno[3,2-b]pyridine

https://huagongshe.com/reaction/889880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CyanideHCID 9032—
ReactantSodium hydrideHCID 24758—
Reactant7-chloro-2-[(R)-3-hydroxypyrrolidine-1-carbonyl]thieno[3,2-b]pyridineHCID 20767758—
SolventTetrahydrofuranHCID 8028—
Product7-chloro-2-[(R)-3-methoxypyrrolidine-1-carbonyl]thieno[3,2-b]pyridineHCID 2076776561%

Reaction Steps

NaH (2.1 g, 53.1 mmol) was added to a solution of (3R)-(3-hydroxy-pyrrolidin-1-yl)-[7-chloro-thieno[3,2-b]pyridin-2-yl]-methanone (5.0 g, 17.7 mmol) in THF (100 mL), at 0° C. The reaction mixture was allowed to stir for 20 min., and MeI (3.26 g, 22.9 mmol) was added dropwise. After 3 h the reaction was treated with saturated aqueous KCN. The aqueous layer was extracted with CH2Cl2. The combined organic layers were dried (Na2SO4), and the solvent was removed under reduced pressure. Purification by flash chromatography on silica gel, eluting with CH2Cl2/MeOH (94:6) afforded the title compound as a white solid (3.2 g, 61%). MS: 297.2/299.2 (MH+); HPLC Rf: 4.25 min.; HPLC purity: 95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995171B2
Source datasetuspto-grants-2006_02
ORD IDord-7eda8dbd196d4f8ba844098a932e8e18
Source noteuspto-grants-2006_02