Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850574Generated: October 29, 2026

3-Boc-9-oxa-3,7-diazabicyclo[3.3.1]nonane → HCID 86686637, compound

https://huagongshe.com/reaction/1850574

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Boc-9-oxa-3,7-diazabicyclo[3.3.1]nonaneHCID 18540412—
Reactant6-(7-cyclopentyl-6-(dimethylcarbamoyl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)nicotinic acidHCID 58315472—
ProductHCID 86686637HCID 8668663734%

Reaction Steps

Following general amide formation method 1, 6-(7-Cyclopentyl-6-dimethylcarbamoyl-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)-nicotinic acid (266 mg, 0.438 mmol, 1.0 eq) was combined with 9-Oxa-3,7-diaza-bicyclo[3.3.1]nonane-3-carboxylic acid tert-butyl ester (100 mg, 0.438 mmol, 1.0 eq) which gave 7-[6-(7-Cyclopentyl-6-dimethylcarbamoyl-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)-pyridine-3-carbonyl]-9-oxa-3,7-diaza-bicyclo[3.3.1]nonane-3-carboxylic acid tert-butyl ester as a light pink powder (90 mg) in 34% yield. MS m/z 605.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957074B2
Source datasetuspto-grants-2015_02
ORD IDord-fdcbdf986882426982a21cde10e38251
Source noteuspto-grants-2015_02