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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455325Generated: November 3, 2026

Dichloromethane → HCID 10992887, compound

https://huagongshe.com/reaction/1455325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantEthyl bromoacetateHCID 7748—
Reactant4-MethylmorpholineHCID 7972—
ReactantN-[(Phenylmethoxy)carbonyl]-L-alanyl-L-alanine hydrazideHCID 13749960—
SolventDimethylformamideHCID 6228—
ProductHCID 10992887HCID 1099288736%

Reaction Conditions

Temperature-10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482379B2
Source datasetuspto-grants-2009_01
ORD IDord-fd5aa05dc49443049d803a9049877616
Source noteuspto-grants-2009_01