HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2-(Benzylcarbamoyl)-1-methylhydrazinyl)acetic acid → 4-benzyl-1-(2-((S)-1-(((S)-1,1-diethoxypropan-2-yl)(quinolin-8-ylmethyl)amino)-1,4-dioxo-4-(tritylamino)butan-2-ylamino)-2-oxoethyl)-1-methylsemicarbazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2-(Benzylcarbamoyl)-1-methylhydrazinyl)acetic acid | HCID 53397489 | — |
| Reactant | (S)-2-amino-N1-((S)-1,1-diethoxypropan-2-yl)-N1-(quinolin-8-ylmethyl)-N4-tritylsuccinamide | HCID 67075012 | — |
| Product | 4-benzyl-1-(2-((S)-1-(((S)-1,1-diethoxypropan-2-yl)(quinolin-8-ylmethyl)amino)-1,4-dioxo-4-(tritylamino)butan-2-ylamino)-2-oxoethyl)-1-methylsemicarbazide | HCID 67088390 | — |
Reaction Steps
According to the procedure described in the synthesis method of Compound II-15, 2-(2-(benzylcarbamoyl)-1-methylhydrazinyl)acetic acid (Compound VI-3) 55 mg (0.23 mmol) was coupled with (S)-2-amino-N1—((S)-1,1-diethoxypropan-2-yl)-N1-(quinolin-8-ylmethyl)-N4-tritylsuccinamide (Compound IV-20) 100 mg (0.16 mmol) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08455488B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-c88e804a55a44fcdb621bb20b5eb6a79 |
| Source note | uspto-grants-2013_06 |