HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indazol-5-amine → HCID 22147946, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indazol-5-amine | HCID 88012 | — |
| Reactant | HCID 22147950 | HCID 22147950 | — |
| Product | HCID 22147946 | HCID 22147946 | — |
Reaction Steps
5-Aminoindazole was coupled with (2-tert-butoxycarbonylamino-ethylamino)-(3-methoxy-phenyl)-acetic acid according to the method described in Example 1. The BOC protecting group was then removed according to the method described in Example 8 to afford compound I-1017. 1H NMR (400 MHz, DMSO-d6) δ 3.02–3.14 (4H, m), 3.80 (3H,s), 4–5 (1H, vbr s), 5.11 (1H, brs), 7.05 (1H,d), 7.20 (2H,m), 7.40 (2H,m), 7.52 (1H,d), 7.5–8 (2H, brs), 8.05 (1H,s), 8.07 (1H,s), 8.2–10.1 (1H, brs), 10.68 (1H,brs), 13.15 (1H,brs); MS (ES+): m/e=340.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07041687B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-de58199f29ec4d328b0419da278ef195 |
| Source note | uspto-grants-2006_05 |