Sodium ethoxide → HCID 54493047, compound
Reaction equation
[CH3:1][C:2]1[S:3][C:4]([CH2:12][CH2:13][CH2:14][C:15]([O:17]CC)=O)=[C:5](C(OCC)=O)[N:6]=1.[O-]CC.[Na+]>>[CH3:1][C:2]1[S:3][C:4]2[CH2:12][CH2:13][CH2:14][C:15](=[O:17])[C:5]=2[N:6]=1Participants
3
Procedure
The compound is prepared from the product obtained in step (a), by cyclization with sodium ethoxide, followed by hydrolysis and decarboxylation of the crude ester. B.p.0.2 =130°-140° C. M.p.=86°-87° C. Overall yield: 26%.
Workup
- customB.p.0.2 =130°-140° C
Sources & evidence
- ORD record
- ord-a3c8a847ba1c43b2b1c37e57ca0f6cd0
- Source dataset
- uspto-grants-1980_06
- Patent number
- US04208420
Reaction notes
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