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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627398Generated: October 30, 2026

8-Oxa-3-azabicyclo[3.2.1]octane → HCID 67354909, compound

https://huagongshe.com/reaction/627398

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Oxa-3-azabicyclo[3.2.1]octaneHCID 12069231—
Reactant6-(7-cyclopentyl-6-(dimethylcarbamoyl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)nicotinic acidHCID 58315472—
ProductHCID 67354909HCID 6735490932.5%

Reaction Steps

Following general amide formation method 3, 6-(7-cyclopentyl-6-(dimethylcarbamoyl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)nicotinic acid (528 mg, 1.34 mmole) was combined with 8-Oxa-3-aza-bicyclo[3.2.1]octane (199 mg, 1.34 mmol) which gave 7-Cyclopentyl-2-[5-(8-oxa-3-aza-bicyclo[3.2.1]octane-3-carbonyl)-pyridin-2-ylamino]-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide (213 mg, 0.435 mmol) in 32.5% yield. 1H NMR (400 MHz, CDCl3) δ ppm 1.74 (m, 8H), 2.07 (m, 5H), 2.58 (m, 2H), 3.17 (s, 7H), 4.81 (dd, 1H), 6.48 (s, 1H), 7.79 (dd, 8.30 (s, 1H), 8.39 (d, 1H), 8.56 (d, 1H), 8.77 (s, 1H) MS m/z 490.5 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309252B2
Source datasetuspto-grants-2016_04
ORD IDord-35d0080f533f401ebb2106a5fb6a8f2b
Source noteuspto-grants-2016_04