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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373411Generated: October 31, 2026

Water → 9-Chloro-2-[4-(3-pyrrolidin-1-yl-propyl)-phenylamino]-5h,7h-benzo[b]pyrimido[4,5-d]-azepin-6-one

https://huagongshe.com/reaction/2373411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant9-Chloro-2-[4-(3-pyrrolidin-1-yl-prop-1-ynyl)-phenylamino]-5h,7h benzo[b]pyrimido[4,5-d]azepin-6-oneHCID 59851312—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product9-Chloro-2-[4-(3-pyrrolidin-1-yl-propyl)-phenylamino]-5h,7h-benzo[b]pyrimido[4,5-d]-azepin-6-oneHCID 59851705—

Reaction Conditions

Temperature22 °C

Reaction Steps

To a solution of 9-chloro-2-[4-(3-pyrrolidin-1-yl-prop-1-ynyl)-phenylamino]-5H,7H benzo[b]pyrimido[4,5-d]azepin-6-one (I-47) (0.082 g, 0.19 mmol) in EtOH (5 mL) was added Pd/C (10% wt, ˜50% H2O, 0.01 g) and the mixture was placed under H2 (1 atm) and stirred for 12 h at 22° C. The reaction mixture was filtered through Celite® and the filtrate concentrated in vacuo to give crude product as a yellow oil. Purification by C-18 RP LC-MS chromatography afforded I-66 (0.046 g, 56%):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459448B2
Source datasetuspto-grants-2008_12
ORD IDord-0343c52c81ac4297bfa226cc320edab9
Source noteuspto-grants-2008_12