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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676759Generated: October 31, 2026

1-Hydroxybenzotriazole → HCID 58015087, compound

https://huagongshe.com/reaction/1676759

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Reactant4-(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-fluoro-benzoic acidHCID 58015083—
ReactantHCID 178484289HCID 178484289—
SolventDimethylformamideHCID 6228—
ProductHCID 58015087HCID 5801508763.8%

Reaction Steps

To a mixture of 0.10 g (0.23 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-fluoro-benzoic acid (I-182) and 6 mL of dimethylformamide was added 0.0499 g (0.37 mmole) of 1-hydroxybenzotriazole, 0.1349 g (0.356 mmole) of 1-[bis(dimethylamino)methylene]-1H-benzotriazolium-3-oxide hexafluorophosphate and 0.0615 g (1.378 mmole) of diisopropylethylamine. The mixture was stirred for 10 minutes, then 0.0728 g (0.349 mmole) of 4-amino-1-Boc-piperidine was added. The reaction mixture was stirred for 2 hours and then concentrated under reduced pressure. The residue was dissolved in 80 mL of ethyl acetate and washed three times with 10 mL of 1M sodium hydroxide, twice with 15 mL of brine, dried, filtered and concentrated under reduced pressure. Purification by silica gel chromatography, eluting with dichloromethane-methanol (gradient, 95:5-90:10) gave 0.0906 g of 4-[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-fluoro-benzoylamino]-piperidine-1-carboxylic acid tert-butyl ester (I-229) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003785B2
Source datasetuspto-grants-2011_08
ORD IDord-66d6c0f45f944348a07daae3883c94ff
Source noteuspto-grants-2011_08