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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850557Generated: October 30, 2026

2-(3,8-Diazabicyclo[3.2.1]octan-8-yl)ethan-1-ol → HCID 86686634, compound

https://huagongshe.com/reaction/1850557

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3,8-Diazabicyclo[3.2.1]octan-8-yl)ethan-1-olHCID 45099440—
Reactant6-(7-cyclopentyl-6-(dimethylcarbamoyl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)nicotinic acidHCID 58315472—
ProductHCID 86686634HCID 8668663459%

Reaction Steps

The 6-(7-cyclopentyl-6-(dimethylcarbamoyl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)nicotinic acid was combined with 2-(3,8-diazabicyclo[3.2.1]octan-8-yl)ethanol following amide formation method 3 which gave 7-cyclopentyl-2-(5-(8-(2-hydroxyethyl)-3,8-diazabicyclo[3.2.1]octane-3-carbonyl)pyridin-2-ylamino)-N,N-dimethyl-7H-pyrrolo[2,3-d]pyrimidine-6-carboxamide (18 mg, 59% yield). 1H NMR (400 MHz, CDCl3) δ ppm 9.00-8.87 (m, 1H) 8.87-8.78 (m, 1H) 8.57 (d, J=8.08 Hz, 1H) 8.44 (s, 1H) 7.79 (dd, J=8.59, 2.53 Hz, 1H) 6.54-6.43 (m, 1H) 4.81 (dq, J=9.09, 8.93 Hz, 1H) 4.51 (br. s., 1H) 3.82-3.49 (m, 4H) 3.40-2.99 (m, 10H) 2.69-2.44 (m, 4H) 2.16-1.99 (m, 4H) 1.91 (d, J=5.56 Hz, 2H) 1.83-1.45 (m, 4H); HR-MS (m/z MH+) 533.30 RT 2.56 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957074B2
Source datasetuspto-grants-2015_02
ORD IDord-76e826592ba54db48178f84d88d3a39c
Source noteuspto-grants-2015_02