HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Benzyl-9-oxa-3,7-diazabicyclo[3.3.1]nonane → HCID 67355729, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Benzyl-9-oxa-3,7-diazabicyclo[3.3.1]nonane | HCID 16036407 | — |
| Reactant | 6-(7-cyclopentyl-6-(dimethylcarbamoyl)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)nicotinic acid | HCID 58315472 | — |
| Product | HCID 67355729 | HCID 67355729 | 43.4% |
Reaction Steps
Following general amide formation method 1, 6-(7-cyclopentyl-6-dimethylcarbamoyl-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)-nicotinic acid (200 mg, 0.507 mmol, 1.0 eq) was combined with 3-benzyl-9-oxa-3,7-diaza-bicyclo[3.3.1]nonane (162 mg, 0.558 mmol, 1.1 eq) (Reference: PCT Int. Appl. 2006137769, 2 Dec. 2006) which gave 2-[5-(7-Benzyl-9-oxa-3,7-diaza-bicyclo[3.3.1]nonane-3-carbonyl)-pyridin-2-ylamino]-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide as solid (131 mg) in 39% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957074B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-ebe6904083364da983df24e5b71fd5c7 |
| Source note | uspto-grants-2015_02 |