HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-({3-bromo-5-[(dipropylamino)carbonyl]benzoyl}amino)-1,2,5-trideoxy-6-S-methyl-1-phenyl-6-thio-D-xylo-hexitol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Trifluoroacetate | HCID 84468 | — |
| Reactant | 3-Bromo-5-[(dipropylamino)carbonyl]Benzoic Acid | HCID 11290370 | — |
| Reactant | (2s,3r,4s)-2-Amino-6-methylsulfanyl-1-phenyl-hexane-3,4-diol | HCID 69747529 | — |
| Product | 2-({3-bromo-5-[(dipropylamino)carbonyl]benzoyl}amino)-1,2,5-trideoxy-6-S-methyl-1-phenyl-6-thio-D-xylo-hexitol | HCID 59067285 | — |
Reaction Steps
The trifluoroacetate salt of (2S,3R,4S)-2-Amino-6-methylsulfanyl-1-phenyl-hexane-3,4-diol (0.1 mmol) was reacted with 5-bromo-N,N-dipropyl-isophthalamic acid as described in method A (addition of an extra equivalent of DIEA to neutralize the amine salt) to give 2-({3-bromo-5-[(dipropylamino)carbonyl]benzoyl}amino)-1,2,5-trideoxy-6-S-methyl-1-phenyl-6-thio-D-xylo-hexitol. MS (ESI+) for C27H37BrN2O4S m/z 567 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06906104B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-3fc1654fff01438fbc4434d88343cea9 |
| Source note | uspto-grants-2005_06 |