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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1512059Generated: October 26, 2026

Acetic Acid → 4-{3-[2-Fluoro-4-((2S,3'S)-2-methyl-[1,3']bipyrrolidinyl-1'-yl)-phenylamino]-propyl}-tetrahydro-pyran-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/1512059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(3-Oxo-propyl)tetrahydro-pyran-4-carboxylic acid methyl esterHCID 58468057—
Reactant2-Fluoro-4-((2S,3'S)-2-methyl-[1,3']bipyrrolidinyl-1'-yl)-phenylamineHCID 67423102—
Solvent1,2-DichloroethaneHCID 11—
Product4-{3-[2-Fluoro-4-((2S,3'S)-2-methyl-[1,3']bipyrrolidinyl-1'-yl)-phenylamino]-propyl}-tetrahydro-pyran-4-carboxylic acid methyl esterHCID 58468077—

Reaction Steps

4-(3-Oxo-propyl)tetrahydro-pyran-4-carboxylic acid methyl ester (135 mg, 0.515 mmol, 1 eq) was dissolved in 2.4 mL of 1,2-dichloroethane. To this was added 2-Fluoro-4-((2S,3′S)-2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenylamine (103 mg, 0.515 mmol, 1 eq) in 6.2 mL of 1,2-dichloroethane. To the combined mixture was added glacial acetic acid (96 mg, 1.6 mmol, 3.1 eq) followed by NaBH(OAc)3 (330 mg, 1.55 mmol, 3 eq). The reaction mixture was stirred at rt for 15 h. The reaction mixture was quenched with water, transferred to a separatory funnel and extracted with CH-2Cl2 (2×100 mL). The combined organics were dried over Na2SO4, concentrated under vacuum and purified by column chromatography on silica gel (40 g column, 6% MeOH in CH2Cl2; 35 mL/min). This gave 130 mg (61%) of the title compound as a beige semi-solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217052B2
Source datasetuspto-grants-2012_07
ORD IDord-6093c12da6dd47d49670b6b95cffdc99
Source noteuspto-grants-2012_07