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Furfural → HCID 178447403, compound

HRID 1647327
Notes
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Reaction equation

HRID 1647327 reaction equation
FC(F)(F)C(O)=O.[NH2:8][C:9]([CH3:45])([CH3:44])[CH2:10][C:11]([NH:13][C@H:14]1[C:20](=[O:21])[N:19]([CH2:22][C:23]2[CH:28]=[CH:27][C:26]([C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=3[C:35]3[NH:39][N:38]=[N:37][N:36]=3)=[CH:25][CH:24]=2)[C:18]2[CH:40]=[CH:41][CH:42]=[CH:43][C:17]=2[S:16][CH2:15]1)=[O:12].[CH:46](=O)[C:47]1[O:51][CH:50]=[CH:49][CH:48]=1>>[O:51]1[CH:50]=[CH:49][CH:48]=[C:47]1[CH2:46][NH:8][C:9]([CH3:45])([CH3:44])[CH2:10][C:11]([NH:13][C@H:14]1[C:20](=[O:21])[N:19]([CH2:22][C:23]2[CH:24]=[CH:25][C:26]([C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=3[C:35]3[NH:39][N:38]=[N:37][N:36]=3)=[CH:27][CH:28]=2)[C:18]2[CH:40]=[CH:41][CH:42]=[CH:43][C:17]=2[S:16][CH2:15]1)=[O:12]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 7362FurfuralHCID 178457467HCID 178457467, compound

Product 1

HCID 178447403HCID 178447403, compound

Procedure

The title compound is prepared from 3-amino-3-methyl-N-[3,4-dihydro-4-oxo-5-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-1,5-benzothiazepin-3(S)-yl]butanamide trifluoroacetate (prepared by the method of M. Fisher, et al, U.S. Pat. No. 5,206,235) and furfuraldehyde by the procedures described in Example 1.

Workup

  1. customprepared by the method of M

Sources & evidence

ORD record
ord-98f164d2964e440fb6788194969cb1bc
Source dataset
uspto-grants-1995_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05430144

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes