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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499029Generated: November 2, 2026

Sodium Acetate → Cyclopropylmethyl-[2-(1H-indol-4-yl)-4-morpholin-4-yl-pyrido[3',2':4,5]furo[3,2-d]pyrimidin-8-ylmethyl]-methyl-amine

https://huagongshe.com/reaction/1499029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(Cyclopropylmethyl)(methyl)amine hydrochlorideHCID 12919210—
ReactantCyclopropyl-[2-(1H-indol-4-yl)-4-morpholin-4-yl-pyrido[3',2':4,5]furo[3,2-d]pyrimidin-8-ylmethyl]-methyl-amineHCID 50991103—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductCyclopropylmethyl-[2-(1H-indol-4-yl)-4-morpholin-4-yl-pyrido[3',2':4,5]furo[3,2-d]pyrimidin-8-ylmethyl]-methyl-amineHCID 50991104—

Reaction Steps

To a solution of compound 23 (as per Example S above) (19 mg, 0.048 mmol, leg), NaBH3CN (6.0 mg, 0.096 mmol. 2 eq), NaBH(OAc)3 (31 mg, 0.144 mmol, 3 eq), NaOAc (15.7 mg, 0.19 mmol, 4 eq) in a mixture of anhydrous CH2Cl2 (2 mL), MeOH (2 mL) and DMF (0.5 mL) was added cyclopropylmethyl-methyl-amine hydrochloride (23 mg, 0.19 mmol, 4 eq) under Ar(g). The reaction mixture was stirred at rt overnight. Solvents were removed in vacuo. Then, the residue was partitioned with H2O (10 mL) and extracted with CH2Cl2 (3×10 mL) and EtOAc (2×10 mL). The combined organic extracts were dried over MgSO4 and the solvent was removed in vacuo. The residue was further purified by silica gel column chromatography with CH2Cl2/MeOH (1:0-47:3) to yield the product, T, as a white solid (8.35 mg, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200007B2
Source datasetuspto-grants-2015_12
ORD IDord-994d382b50ae4f1282b3211768e3fb70
Source noteuspto-grants-2015_12