HCID 59556943, compound → HCID 67105280, compound
Reaction equation
[Cl:1][C:2]1[CH:9]=[C:8]([N:10]2[CH:14]([CH2:15][OH:16])[C:13](=[O:17])[C:12]([CH3:19])([CH3:18])[C:11]2=[O:20])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5].C([BH-](C(CC)C)C(CC)C)(CC)C.[Li+].C1COCC1>>[Cl:1][C:2]1[CH:9]=[C:8]([N:10]2[C@H:14]([CH2:15][OH:16])[C@H:13]([OH:17])[C:12]([CH3:18])([CH3:19])[C:11]2=[O:20])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5]Participants
3
Procedure
Using 2-chloro-4-[5-(hydroxymethyl)-3,3-dimethyl-2,4-dioxopyrrolidin-1-yl]benzonitrile (80 mg) and lithium tri(sec-butyl)borohydride-THF solution (0.82 mL, 1 mol/L), and in the same manner as in Example 5, the title compound was obtained as colorless crystals (yield: 45.4 mg, 56%).
Sources & evidence
- ORD record
- ord-9622c9ee44d54667b1daaf27a22559d8
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07834051B2
Reaction notes
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