HuagongsheHuagongshe Chemistry Print Report · For research reference only
8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, hydrazide → 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[3-[[(1,1-dimethylethoxy)carbonyl](2-thienylmethyl)-amino]-1-oxopropyl]hydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, hydrazide | HCID 13560461 | — |
| Reactant | 3-{[(t-Butoxy)carbonyl][(thiophen-2-yl)methyl]amino}propanoic acid | HCID 23369387 | — |
| Solvent | Water | HCID 962 | — |
| Product | 8-chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-[3-[[(1,1-dimethylethoxy)carbonyl](2-thienylmethyl)-amino]-1-oxopropyl]hydrazide | HCID 86748363 | — |
Reaction Steps
1.1 mmol of 3-[[(1,1-dimethylethoxy)carbonyl](2-thienylmethyl)amino]-propanoic acid (16), prepared as described above in Example 16, was reacted with 8-chlorodibenz[b,f][1,4]-oxazepine-10(11H)-carboxylic acid, hydrazide (1), prepared as described above in Example 1, in the same manner described in Example 9. The yield of product was 0.31 g (51%). Analysis calculated for C27H29N4O5SCl 0.25 H2O (M.W. 561.57): C, 57.29.; H, 5.34; N, 9.90. Found: C, 57.42; H, 5.40; N, 9.96.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05576315 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-4b7327b9215f406e93cb60afc5859c9c |
| Source note | uspto-grants-1996_11 |