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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220723Generated: October 26, 2026

2486-69-3 → 4-(9-Cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[5,4-b][1,4]diazepin-2-ylamino)-3-methoxybenzoic acid

https://huagongshe.com/reaction/220723

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2486-69-3HCID 288057—
Reactant2-Chloro-9-cyclopentyl-7,7-difluoro-5-methyl-8,9-dihydro-5H-pyrimido[4,5-B][1,4]diazepin-6(7H)-oneHCID 57955574—
CatalystHydrochloric AcidHCID 313—
SolventIsopropanolHCID 3776—
Product4-(9-Cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[5,4-b][1,4]diazepin-2-ylamino)-3-methoxybenzoic acidHCID 25252905—

Reaction Steps

2-Chloro-9-cyclopentyl-7,7-difluoro-5-methyl-8,9-dihydro-5H-pyrimido[5,4-b][1,4]diazepin-6(7H)-one (obtained above), 4-amino-3-methoxy benzoic acid (334 mg, 2 mmol), i-PrOH (10 mL) and conc. HCl (10 drops) were heated to 100° C. overnight. The reaction mixture was then cooled to room temperature, concentrated and redissolved in MeOH, treated with NaOH and refluxed for 1 hr. After which, it was concentrated, acidified with HCl and filtered to give the title as a tan solid (300 mg). [M+H] calc'd for C21H23F2N5O4, 448; found 448.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202990B2
Source datasetuspto-grants-2012_06
ORD IDord-8936ff2a70b34497bcb94b245797cc00
Source noteuspto-grants-2012_06