HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrimidine-5-carboxaldehyde → HCID 11689060, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrimidine-5-carboxaldehyde | HCID 2761034 | — |
| Reactant | 6-chloro-N-(piperidin-4-yl)thieno[2,3-d]pyrimidin-4-amine | HCID 57933147 | — |
| Product | HCID 11689060 | HCID 11689060 | — |
Reaction Steps
The title compound was prepared (119 mg, 45%) from 6-chloro-N-(piperidin-4-yl)thieno[2,3-d]pyrimidin-4-amine (200 mg, 0.74 mmol) and pyrimidine-5-carbaldehyde (80 mg, 0.74 mmol) by following the general procedure described for Preparation 11. 1H NMR (400 MHz, CDCl3): δ 9.05 (s, 1H), 8.65 (s, 2H), 8.35 (s, 1H), 7.00 (s, 1H), 5.50 (bs, 1H), 4.10 (m, 1H), 3.45 (s, 2H), 2.80 (m, 2H), 2.20 (m, 2H), 2.00 (m, 2H), 1.50 (m, 2H). MS (ESI) m/z: Calculated: 360.09; Observed: 361.1 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07612078B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-ac2bf680e6ab40c7826a27656ab69497 |
| Source note | uspto-grants-2009_11 |