HCID 22556513, compound → HCID 9799912, compound
Reaction equation
[C:1]([C:3]1[O:10][C:9]2[CH:8]=[C:7]([C:11]([OH:13])=O)[NH:6][C:5]=2[CH:4]=1)#[N:2].Cl.[NH2:15][C@@H:16]([CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[C:17]([N:19]1[CH2:22][CH:21]([OH:23])[CH2:20]1)=[O:18]>>[CH2:24]([C@H:16]([NH:15][C:11]([C:7]1[NH:6][C:5]2[CH:4]=[C:3]([C:1]#[N:2])[O:10][C:9]=2[CH:8]=1)=[O:13])[C:17]([N:19]1[CH2:22][CH:21]([OH:23])[CH2:20]1)=[O:18])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1Participants
3
Procedure
2-Cyano-4H-furo[3,2-b]pyrrole-5-carboxylic acid and (2S)-amino-1-(3-hydroxy-azetidin-1-yl)-3-phenyl-propan-1-one hydrochloride were coupled according to Procedure B (reaction mixture partitioned between ethyl acetate and water prior to acidic washing).
Workup
- customreaction mixture
- custompartitioned between ethyl acetate and water
- washto acidic washing)
Sources & evidence
- ORD record
- ord-a42b29f41e1c4c39b7c8dbed63a4bed6
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06576653B2
Reaction notes
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