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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676839Generated: October 29, 2026

Diisopropylethylamine → HCID 178492711, compound

https://huagongshe.com/reaction/1676839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttrans-4-(4-(Cyclopropylmethyl)piperazin-1-yl)cyclohexanamineHCID 11586738—
Reactant4-(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—
SolventDimethylformamideHCID 6228—
ProductHCID 178492711HCID 178492711—
ProductHCID 178492712HCID 178492712—

Reaction Steps

To a mixture of 0.08 g (0.18 mmole) of 4-(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-ylamino)-3-methoxy-benzoic acid (I-22), 0.19 mL (1.1 mmole) of ethyldiisopropyl amine and 0.068 mg (0.20 mmole) of the cis/trans mixture of 4-(4-cyclopropylmethyl-piperazin-1-yl)-cyclohexylamine with trihydrochloride in 2.0 mL of dimethylformamide was added 0.085 g (0.20 mmole) of 1-(di-1-pyrrolidinylmethylene)-1H-benzotriazolium 3-oxide hexafluorophosphate. The mixture was stirred at room temperature for 1 hour, then diluted with 10 mL of ice water. The resulting solid was collected by filtration, washed with saturated sodium carbonate and water, and dried under vacuum. Purification by silica gel chromatography, eluting with dichloromethane-methanol (gradient, 100:0-70:30) gave 0.026 g of 4-(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-ylamino)-N-[cis-4-(4-cyclopropylmethyl-piperazin-1-yl)-cyclohexyl]-3-methoxy-benzamide (I-299) (Rf: 0.56 in dichloromethane:methanol 7:3) as a white solid, and 0.063 g of 4-(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,4]diazepin-2-ylamino)-N-[trans-4-(4-cyclopropylmethyl-piperazin-1-yl)-cyclohexyl]-3-methoxy-benzamide (I-300) (Rf: 0.44 in dichloromethane:methanol 7:3) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003785B2
Source datasetuspto-grants-2011_08
ORD IDord-8861a5f01b5f431e83e282232397f45c
Source noteuspto-grants-2011_08