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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172056Generated: October 26, 2026

Acetonitrile → HCID 178499066, compound

https://huagongshe.com/reaction/1172056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium HydroxideHCID 14798—
ReactantSodium NitriteHCID 23668193—
Reactant6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-methoxypyrimidine-4-carboxylic acid methyl esterHCID 59126928—
SolventSulfuric AcidHCID 1118—
ProductHCID 178499066HCID 17849906675%

Reaction Conditions

Temperature25 °C

Reaction Steps

6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-methoxypyrimidine-4-carboxylic acid methyl ester (200 mg, 0.61 mmol) was dissolved in 20 mL of 9 molar H2SO4 plus 5 mL acetonitrile and treated in portions with NaNO2 (150 mg, 2.2 mmol). After the addition was complete, the mixture was stirred for 30 minutes at 25° C., cooled in ice-salt and treated carefully with 50% NaOH to bring the pH to ca 0.8. The precipitate was taken up by extracting with two 15 mL portions of EtOAc and the combined extracts were washed with 10 mL sat. NaCl, dried (Na2SO4) and evaporated to give the title product 150 mg (75%). Mp: 177-179° C. MS m/z 342; 1H NMR (DMSO-d6): δ 7.81 (m, 1H), 7.31 (m, 1H), 4.05 (s, 3H), 4.01 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833940B2
Source datasetuspto-grants-2010_11
ORD IDord-f7a8adda4ac14ae2bee2ce4706ab7759
Source noteuspto-grants-2010_11