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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734443Generated: October 30, 2026

Triphenylphosphine → methyl (5-{3-[(2-chloro-5-fluoro-4-pyrimidinyl)(methyl)amino]propoxy}-1H-indol-1-yl)acetate

https://huagongshe.com/reaction/734443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactantmethyl (5-hydroxy-1H-indol-1-yl)acetateHCID 20770839—
Reactant3-[(2-Chloro-5-fluoro-4-pyrimidinyl)(methyl)amino]-1-propanolHCID 57845518—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Productmethyl (5-{3-[(2-chloro-5-fluoro-4-pyrimidinyl)(methyl)amino]propoxy}-1H-indol-1-yl)acetateHCID 5799221756.7%

Reaction Steps

To a solution of 3-[(2-chloro-5-fluoro-4-pyrimidinyl)(methyl)amino]-1-propanol (Example 83, 0.60 g, 2.73 mmol) and methyl (5-hydroxy-1H-indol-1-yl)acetate (Example 9, 0.37 g, 1.82 mmol) in dichloromethane (9 mL) was added triphenylphosphine (0.70 g, 2.73 mmol) and 1,1′-(azodicarbonyl)-dipiperidine (0.72 g, 2.73 mmol) under argon. The golden yellow mixture was stirred at rt for 18 h. The desired product (0.42 g, 56%) was obtained after column chromatography (67% hexanes in EtOAc). 1H NMR (300 MHz, CD2Cl2) δ 7.85 (d, 1H), 7.15-7.07 (m, 3H), 6.88-6.83 (m, 1H), 6.47-6.46 (m, 1H), 4.85 (s, 2H), 4.07 (t, 2H), 3.84 (t, 2H), 3.76 (s, 3H), 3.26 (d, 3H), 2.20-2.13 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592361B2
Source datasetuspto-grants-2009_09
ORD IDord-e1a141cbb23c46d6ae93dca461593ff1
Source noteuspto-grants-2009_09