Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | N-[(Phenylmethoxy)carbonyl]-L-alanyl-L-alanine hydrazide | HCID 13749960 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10992887 | HCID 10992887 | 36% |
Reaction Steps
Ethyl bromoacetate (1.1 eq) was added dropwise to a stirred solution of Cbz-Ala-Ala-NHNH2 (1 eq) and NMM (1.1 eq) in DMF that was cooled to −10° C. The resulting solution was stirred for 30 min at −10° C., after which the mixture was allowed to react at room temperature for 36 hours. The DMF was evaporated, and the residue was purified on a silica gel column using 1:9 MeOH:CH2Cl2 as the eluting solvent system to afford 4a as a white solid (yield=36%). 1H NMR (DMSO-d6): 1.18 (t, 9H, CH3), 3.5 (d, 2H, NCH2COOEt), 4.0-4.15 (m, 3H, α-H and OCH2CH3), 4.2 (m, 1H), α-H), 5.03 (m, 2H, Cbz), 5.18 (m, 1H, NH), 7.22-7.40 (m, 5H, Ph), 7.4-7.5 (d, 1H, NH), 7.9 (m, 1H, NH), 9.35 (m, 1H, NH). MS (FAB) m/z 395 [(M+1)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07482379B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-fd5aa05dc49443049d803a9049877616 |
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| Source note | uspto-grants-2009_01 |
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