Isocaproaldehyde → HCID 69590994, compound

HRID 2414955Notes

Reaction equation

HRID 2414955 reaction equation
[CH2:1]([C@:3]1([OH:29])[C:26]2[CH:25]=[C:24]3[N:10]([CH2:11][C:12]4[C:13]3=[N:14][C:15]3[CH:16]=[C:17]([F:23])[CH:18]=[C:19]([F:22])[C:20]=3[CH:21]=4)[C:9](=[O:27])[C:8]=2[CH2:7][O:6][C:5](=[O:28])[CH2:4]1)[CH3:2].[CH3:30][CH:31]([CH3:36])[CH2:32][CH2:33]C=O>>[CH2:1]([C@:3]1([OH:29])[C:26]2[CH:25]=[C:24]3[N:10]([CH2:11][C:12]4[C:13]3=[N:14][C:15]3[CH:16]=[C:17]([F:23])[CH:18]=[C:19]([F:22])[C:20]=3[C:21]=4[CH2:33][CH2:32][CH:31]([CH3:36])[CH3:30])[C:9](=[O:27])[C:8]=2[CH2:7][O:6][C:5](=[O:28])[CH2:4]1)[CH3:2]

Participants

3

Procedure

The product of Example 100 is treated with 4-methylpentanal according to a procedure similar to Stage 95e in order to produce the expected solid.

Workup

  1. customto produce the expected solid

Sources & evidence

ORD record
ord-da1805bea0d54787a2c543e4b8e6379e
Source dataset
uspto-grants-2004_11
Patent number
US06815546B2

Reaction notes

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