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2-(3-(methylamino)propyl)-1H-benzimidazole → HCID 68748561, compound

HRID 919196
Notes
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Reaction equation

HRID 919196 reaction equation
[F:1][C:2]1([F:21])[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([F:12])[CH:10]=2)[C@H:5]([CH:13]([CH3:15])[CH3:14])[C@:4]([CH2:17][C:18](O)=[O:19])([OH:16])[CH2:3]1.[NH:22]1[C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][C:25]=2[N:24]=[C:23]1[CH2:31][CH2:32][CH2:33][NH:34][CH3:35].N1C2C=CC=CC=2N=C1CCCN(C)C(=O)C[C@@]1(O)C([2H])([2H])C([2H])([2H])C2C(=CC=C(F)C=2)[C@@H]1C(C)C>>[NH:22]1[C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][C:25]=2[N:24]=[C:23]1[CH2:31][CH2:32][CH2:33][N:34]([CH3:35])[C:18](=[O:19])[CH2:17][C@@:4]1([OH:16])[CH2:3][C:2]([F:1])([F:21])[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([F:12])[CH:10]=2)[C@@H:5]1[CH:13]([CH3:15])[CH3:14]
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 31454002-(3-(methylamino)propyl)-1H-benzimidazoleHCID 58451460N-(3-(1H-Benzo[d]imidazol-2-yl)propyl)-N-methyl-2-((1S,2S)-3,3,4,4-tetradeutero-6-fluoro-2-hydroxy-1-isopropyl-1,2,3,4-tetrahydronaphthalen-2-yl)acetamideHCID 687500552-((1S,2R)-4,4,6-Trifluoro-2-hydroxy-1-isopropyl-1,2,3,4-tetrahydronaphthalen-2-yl)acetic acid

Product 1

HCID 68748561HCID 68748561, compound

Procedure

Intermediate 17d is prepared from 15c and 16e in a manner analogous to that of Example 2, step 1 for 17b.

Sources & evidence

ORD record
ord-8675069eea104d26aa1d6734f64b0237
Source dataset
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09273009B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes