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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607238Generated: October 29, 2026

3-(2-Amino-4-methyl-phenylsulfanyl)-phenol → 3-[4-Methyl-2-(7-propyl-pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenol

https://huagongshe.com/reaction/607238

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-Amino-4-methyl-phenylsulfanyl)-phenolHCID 57469906—
ReactantN'-(3-Cyano-6-propyl-pyridin-2-yl)-N,N-dimethyl-formamidineHCID 66808626—
SolventAcetic AcidHCID 176—
Product3-[4-Methyl-2-(7-propyl-pyrido[2,3-d]pyrimidin-4-ylamino)-phenylsulfanyl]-phenolHCID 66808323—

Reaction Conditions

Temperature130 °C

Reaction Steps

3-(2-amino-4-methyl-phenylsulfanyl)-phenol (49 mg 0.231 mmol) and the product from Example 128A (50 mg, 0.231 mmol) were dissolved in acetic acid (1 mL) and heated to 130° C. for 1.5 hours. After cooling to room temperature a solid in the acetic acid solvent appeared which was collected by filtration to provide the title compound as an acetic acid salt (78 mg, 68%). 1H NMR (300 MHz, DMSO-D6) δ ppm: 0.95 (t, J=7.3 Hz, 3H), 1.79 (m, 2H), 1.88 (s, 6H), 2.40 (s, 3H), 2.88 (t, J=7.6 Hz, 2H), 6.57 (m, 3H), 7.00 (t, J=7.7 Hz, 1H), 7.13 (m, 1H), 7.26 (d, J=7.7 Hz, 1H), 7.38 (s, 1H), 7.51 (d, J=8.5 Hz, 1H), 8.50 (s, 1H), 8.70 (d, J=8.5 Hz, 1H); MS (ESI)+ m/z 403 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915411B2
Source datasetuspto-grants-2011_03
ORD IDord-5cc75d9f96af449f8d14b10cd0e7b2a1
Source noteuspto-grants-2011_03