HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178502362, compound → HCID 178502362, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178502362 | HCID 178502362 | — |
| Reactant | HCID 178502367 | HCID 178502367 | — |
| Product | Ammonium Acetate | HCID 517165 | — |
| Product | HCID 178502362 | HCID 178502362 | 87% |
| Product | HCID 178502367 | HCID 178502367 | — |
Reaction Steps
Phenylmethyl (8S)-8-(4-{4′-[2-((2S)-1-{N-[(methyloxy)carbonyl]-L-valyl}-2-pyrrolidinyl)-1H-imidazol-4-yl]-4-biphenylyl}-1H-imidazol-2-yl)-1,4-dithia-7-azaspiro[4.4]nonane-7-carboxylate (Intermediate 38) (497 mg, 87%) was obtained from phenylmethyl (8S)-8-({[2-(4′-{2-[(2S)-1-((2S)-3-methyl-2-{[(methyloxy)carbonyl]amino}butanoyl)-2-pyrrolidinyl]-1H-imidazol-4-yl}-4-biphenylyl)-2-oxoethyl]amino}carbonyl)-1,4-dithia-7-azaspiro[4.4]nonane-7-carboxylate (Intermediate 37) (584 mg, 0.71 mmol) and ammonium acetate (546 mg, 7.1 mmol), following the similar procedure outlined in the preparation of Intermediate (22). ES LC-MS m/z=806.4 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09150587B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-b7f8ea4a878347a6bbf23883ef1ed8ee |
| Source note | uspto-grants-2015_10 |