HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850586Generated: October 30, 2026
HCID 67355362, compound → HCID 67354780, compound
https://huagongshe.com/reaction/1850586
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 67355362 | HCID 67355362 | — |
| Reactant | HCID 86686640 | HCID 86686640 | — |
| Product | HCID 67354780 | HCID 67354780 | 63.5% |
Reaction Steps
Following general N—C coupling procedure 1, 7-(3-tert-Butyl-phenyl)-2-chloro-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide (100 mg, 0.280 mmol, 1.0 eq) was combined with 3-(6-Amino-pyridine-3-carbonyl)-3,8-diaza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester (93 mg, 0.280 mmol, 1.0 eq) to give 3-{6-[7-(3-tert-Butyl-phenyl)-6-dimethylcarbamoyl-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino]-pyridine-3-carbonyl}-3,8-diaza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester (116 mg) in 60% yield. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.32 (s, 9H) 1.43 (s, 9H) 1.59 (br. s., 2H) 1.81 (br. s., 2H) 2.86 (br. s., 3H) 2.94 (br. s., 3H) 4.12 (br. s., 2H) 6.91 (s, 1H) 7.37-7.43 (m, 2H) 7.45-7.58 (m, 2H) 7.67 (dd, J=8.84, 2.27 Hz, 1H) 8.32 (dd, J=5.81, 2.78 Hz, 2H) 8.96 (s, 1H) 10.05 (s, 1H). MS m/z 653.7 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957074B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-2b5e0c837db146a4bb69ff09fcf48073 |
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| Source note | uspto-grants-2015_02 |
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