HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-BOC-3-Aminopiperidine → HCID 66958099, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-BOC-3-Aminopiperidine | HCID 545809 | — |
| Reactant | 3-(7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-thiophene-2-carboxylic acid benzylamide | HCID 50923861 | — |
| Product | HCID 66958099 | HCID 66958099 | 14% |
Reaction Steps
The title compound was prepared in an analogous manner as 3-(7H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-thiophene-2-carboxylic acid benzylamide using tert-butyl 3-aminopiperidine-1-carboxylate instead of benzylamine and obtained in 14% yield. 1H NMR (DMSO-d6) 11.96 (br s, 1H), 11.39 (br s, 1H), 8.47 (d, J=5.8 Hz, 1H), 8.38 (s, 1H), 8.09-8.01 (m, 1H), 7.78 (d, J=4.8 Hz, 1H), 7.38-7.14 (m, 1H), 6.48-6.43 (m, 1H), 3.91-3.75 (m, 3H), 2.80-2.62 (m, 3H), 1.92-1.84 (m, 1H), 1.75-1.66 (m, 1H), 1.65-1.54 (m, 1H), 1.40 (s, 9H); MS (m/z) 443 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09023847B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-8e26ff6c492e46c691a0826be82fd27b |
| Source note | uspto-grants-2015_05 |