2-Thienylacetonitrile → HCID 11964707, compound
Reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]([CH:11]=O)=[CH:3][CH:2]=1.[S:13]1[CH:17]=[CH:16][CH:15]=[C:14]1[CH2:18][C:19]#[N:20]>>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4](/[CH:11]=[C:18](/[C:14]2[S:13][CH:17]=[CH:16][CH:15]=2)\[C:19]#[N:20])=[CH:3][CH:2]=1Participants
3
Procedure
4-Quinolinecarboxaldehyde (157 mg) was condensed with 2-thiopheneacetonitrile (123 mg) through Method B (production step 3), to thereby yield the target product (yield: 175 mg, 67%).
Sources & evidence
- ORD record
- ord-0dce3098245b453fa8ef3abc4242c74a
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08697742B2
Reaction notes
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