HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865331Generated: October 29, 2026
HCID 22905128, compound → HCID 178481553, compound
https://huagongshe.com/reaction/865331
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22905128 | HCID 22905128 | — |
| Reactant | HCID 178481555 | HCID 178481555 | — |
| Product | HCID 178481553 | HCID 178481553 | — |
Reaction Steps
1-methyl-4-(2-carboxyethyl)-7-(5-guanidino-1-pentyl)-3,4-dihydro-1H-1,4-benzodiazepine-2,5-dione was prepared by the method described in Example 2. Thus, 18 mgs 1-methyl-4-(2-carboxyethyl)-7-(5-amino-1-pentyl)-3,4-dihydro-1H-1,4-benzodiazepine-2,5-dione ylelded 17 mgs (87%) 1-methyl-4-(2-carboxyethyl)-7-(5-guanidino-1-pentyl)-3,4-dihydro-1H-1,4-benzodiazepine-2,5-dione trifluoracetate (1/2" C-18 reverse-phase column, eluting with a solvent gradient of 10:90 methanol(0.1% trifluoracetic acid)/water (0.1% trifluoracetic acid), time 0 to 10 min, to 50:50 methanol(0.1% trifluoracetic acid)/water (0.1% trifluoracetic acid), time 10 min to 40 min, flow=10 ml/min, Rt =38.5 min, un detection 254 nm). HRMS (FAB) molecular ion m/z=390.2132 (cald. C19H27N5O4, 390.2182)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05565449 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-eba5135338934029966f188bcb1b4b7b |
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| Source note | uspto-grants-1996_10 |
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