Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014565Generated: October 25, 2026

Diisopropylethylamine → 2-({2-chloro-6-methyl-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)-6-fluorobenzoic acid

https://huagongshe.com/reaction/1014565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-6-fluorobenzoic acidHCID 521142—
Reactant2,4-dichloro-6-methyl-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidineHCID 58398917—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
Product2-({2-chloro-6-methyl-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)-6-fluorobenzoic acidHCID 5944184866%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a suspension of 2,4-dichloro-6-methyl-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidine (500 mg, 1.40 mmol) and 2-amino-6-fluorobenzoic acid (218 mg, 1.40 mmol) in isopropanol (15 mL) was added diisopropylethylamine (907 mg, 7.02 mmol) and the mixture was heated at 85° C. for ˜72 h. The reaction was diluted with EtOAc (100 ml) and washed with a solution of 1N HCl, a saturated solution of sodium bicarbonate and a saturated solution of NaCl. Solid began to crash out on addition of brine. Ether was added to force everything out of solution and also water was added to ensure NaCl was all in solution. The solids were filtered and dried under reduced pressure to afford 2-({2-chloro-6-methyl-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)-6-fluorobenzoic acid (439 mg, 0.924 mmol) as a pale yellow solid. ESIMS (M+H)+=475.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-b062c54d9e0d46028f4c5463e6cbb81b
Source noteuspto-grants-2011_07