HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl-2-{[4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)benzoyl]amino}-3-methylbutanoate → 2-{[4-(5-Cyano-7-isopropyl-1,3-benzoxazol-2-yl)benzoyl]amino}-3-methylbutanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl-2-{[4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)benzoyl]amino}-3-methylbutanoate | HCID 25151228 | — |
| Reactant | 4-(5-Cyano-7-isopropylbenzo[d]oxazol-2-yl)benzoic acid | HCID 57369945 | — |
| Product | 2-{[4-(5-Cyano-7-isopropyl-1,3-benzoxazol-2-yl)benzoyl]amino}-3-methylbutanoic acid | HCID 25152785 | — |
Reaction Steps
The title compound was prepared from methyl-2-{[4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)benzoyl]amino}-3-methylbutanoate (EXAMPLE 29) using procedure analogous to that described in INTERMEDIATE 2, Step C. Mass spectrum (ESI) 406.20 (M+1). 1H NMR (500 MHz, CDCl3): δ 8.19 (d, J=8.4 Hz, 2H), 7.89 (d, J=8.4 Hz, 2H), 7.79 (d, J=1.4 Hz, 1H), 7.38 (s, 1H), 7.02 (d, J=8.4 Hz, 2H), 4.59 (m, 1H), 3.45 (m, 1H), 2.2 m, 1H), 1.32 (d, J=7.10 Hz, 6H), 0.91 (t, J=6.3 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436028B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-a9ce1d6c0ff04e2389eca36dd3a3f827 |
| Source note | uspto-grants-2013_05 |