HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → HCID 25007433, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | m-Xylyl bromide | HCID 12099 | — |
| Reactant | 5-(Piperidin-4-ylmethoxy)quinazoline-2,4-diamine | HCID 57576565 | — |
| Product | HCID 25007433 | HCID 25007433 | 84% |
Reaction Steps
The benzylamine was obtained by reacting 5-(piperidin-4-ylmethoxy)quinazoline-2,4-diamine (75 mg; 0.27 mmol) and 3-methylbenzyl bromide (60 mg; 0.32 mmol) via Method BB to yield 86 mg. (84% yield). 1HNMR (400 MHz, DMSO-d6) δ 7.34 (t, J=8.0 Hz, 1H), 7.2 (m, 3H), 7.07 (m, 3H), 6.76 (d, J=8.4 Hz, 1H), 6.52 (d, J=8.0 Hz, 1H), 5.94 (br s, 2H), 3.98 (d, J=6.0 Hz, 2H), 3.42 (s, 2H), 2.83 (br d, J=11.2 Hz, 2H), 2.29 (s, 3H), 1.8 (m, 5H), 1.36 (m, 2H). MS m/z (ESI) 378 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07985755B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-94b81ef902c24630be9706de97ee21a2 |
| Source note | uspto-grants-2011_07 |