HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 6986599, compound → HCID 59489950, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 6986599 | HCID 6986599 | — |
| Reactant | HCID 178451959 | HCID 178451959 | — |
| Product | HCID 59489950 | HCID 59489950 | 89.2% |
Reaction Steps
This product was prepared from (S)-4-(3,4-dichlorophenyl)-2-((dimethylamino)methylene)-3,4-dihydronaphthalen-1(2H)-one (1.45 mmol) and (R)-tert-butyl 3-guanidinopiperidine-1-carboxylate hydrochloride salt (3.62 mmol) under the condition described in the general procedure 1 to afford (R)-tert-butyl 3-((S)-6-(3,4-dichlorophenyl)-5,6-dihydrobenzo[h]quinazolin-2-ylamino)piperidine-1-carboxylate (0.68 g) as a light yellow solid. M.p.=85-87° C. 1H NMR 400 MHz (DMSO-d6) δ 8.29 (bs, 1 H), 8.12 (s, 1 H), 7.50-7.35 (m, 4 H), 7.08 (s, 1 H), 7.02-6.98 (m, 2 H), 4.39 (t, J=5.2 Hz, 1 H), 3.74 (bs, 2 H), 3.12-3.04 (m, 2 H), 2.90-2.84 (m, 2 H), 1.89-1.51 (m, 3 H), 1.38-1.24 (m, 11 H). LCMS m/e 525 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08357694B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-15fcd1f0546949b28afc241f7d64134c |
| Source note | uspto-grants-2013_01 |