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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063216Generated: November 2, 2026

Acetic Acid → (7-Chloro-thieno[3,2-b]pyridin-2-yl)-(6-dimethylamino-3-aza-bicyclo[3.1.0]hex-3-yl)-methanone

https://huagongshe.com/reaction/1063216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(6-Amino-3-aza-bicyclo[3.1.0]hex-3-yl)-(7-chloro-thieno[3,2-b]pyridin-2-yl)-methanoneHCID 22278660—
SolventAcetonitrileHCID 6342—
Product(7-Chloro-thieno[3,2-b]pyridin-2-yl)-(6-dimethylamino-3-aza-bicyclo[3.1.0]hex-3-yl)-methanoneHCID 2227861316%

Reaction Steps

NaBH3CN (211 mg, 3.36 mmol) was added to a solution of (6-amino-3-aza-bicyclo[3.1.0]hex-3-yl)-(7-chloro-thieno[3,2-b]pyridin-2-yl)-methanone (250 mg, 0.85 mmol) and formaldehyde (1.14 mL, 17 mmol) in CH3CN at 0° C. After 30 min AcOH (0.5 mL) was added and the reaction mixture was allowed to warm to room temperature. After 1 h the reaction mixture was concentrated, and the resulting residue was dissolved in H20. The resulting aqueous layer was adjusted to pH 9 with 6N NaOH. The resulting solution was extracted with CH2Cl2 (2×) and the combined organic extracts were dried over Na2SO4, filtered, then concentrated. The resulting material was purified on silica gel by flash column chromatography CH2Cl2/MeOH (85/15) to afford the title compound as a white solid (44 mg, 16%). MS: 322.2/324.2 (MH+); HPLC Rf: 3.62 min.; HPLC purity 95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964961B2
Source datasetuspto-grants-2005_11
ORD IDord-856601517c5d4c1db80d416bdd335280
Source noteuspto-grants-2005_11