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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092816Generated: October 31, 2026

Diisopropylethylamine → Methyl 6-(cis-4-Aminotetrahydrofuran-3-ylamino)-4-cyano-2-(m-tolylamino)nicotinate

https://huagongshe.com/reaction/2092816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactantcis-3,4-TetrahydrofurandiamineHCID 14171649—
ReactantMethyl 6-chloro-4-cyano-2-(m-tolylamino)nicotinateHCID 58317587—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductMethyl 6-(cis-4-Aminotetrahydrofuran-3-ylamino)-4-cyano-2-(m-tolylamino)nicotinateHCID 6723920773%

Reaction Steps

To a solution of methyl 6-chloro-4-cyano-2-(m-tolylamino)nicotinate (40 mg, 0.133 mmol) in DMF (1 mL) was added DIPEA (0.046 mL, 0.265 mmol) and (3R,4S)-tetrahydrofuran-3,4-diamine (13.54 mg, 0.133 mmol). The mixture was stirred at RT overnight. Additional amine was added and the reaction mixture was stirred at RT for an additional day. The reaction mixture was diluted in MeOH (10 mL) and purified by reverse phase preparative HPLC. The fractions were collected and ACN was removed via rotary evaporation. The resulting aq solution was neutralized with saturated aq NaHCO3 and washed with EtOAc (2×200 mL), dried over Na2SO4, and filtered. The organic phase was stripped to dryness via rotary evaporation to yield the title compound (35.5 mg, 73%). [M+H] calc'd for C19H21N5O3, 368. found, 368.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440689B2
Source datasetuspto-grants-2013_05
ORD IDord-4ef09cb5cbcb4b0e94bc7dbeabf392bd
Source noteuspto-grants-2013_05