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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627363Generated: October 27, 2026

6-Aminopyridazine-3-carboxylic acid → 3-(6-Amino-pyridazine-3-carbonyl)-3,8-diaza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/627363

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Aminopyridazine-3-carboxylic acidHCID 12200479—
Reactant8-Boc-3,8-diaza-bicyclo(3.2.1)octaneHCID 15740908—
Product3-(6-Amino-pyridazine-3-carbonyl)-3,8-diaza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl esterHCID 6735534751%

Reaction Steps

Following general amide formation method 1, 6-amino-pyridazine-3-carboxylic acid (212 mg, 1.0 mmol) was combined with 3,8-diaza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester (139 mg, 1.0 mmol), which gave 3-(6-Amino-pyridazine-3-carbonyl)-3,8-diaza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester as a white solid (169 mg, 0.51 mmol) in 51% yield. MS m/z 334.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309252B2
Source datasetuspto-grants-2016_04
ORD IDord-866e214981d340a893ab645c48da732f
Source noteuspto-grants-2016_04