Thionyl Chloride → HCID 69701519, compound
Reaction equation
O[CH:2]([C:10]1[CH:15]=[CH:14][C:13]([C:16]2[N:21]3[CH2:22][CH2:23][C:24]4[NH:25][C:26](=[O:29])[CH:27]=[CH:28][C:19]([C:20]=43)=[CH:18][N:17]=2)=[CH:12][CH:11]=1)[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.S(Cl)([Cl:32])=O>>[Cl:32][CH:2]([C:10]1[CH:15]=[CH:14][C:13]([C:16]2[N:21]3[CH2:22][CH2:23][C:24]4[NH:25][C:26](=[O:29])[CH:27]=[CH:28][C:19]([C:20]=43)=[CH:18][N:17]=2)=[CH:12][CH:11]=1)[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1Participants
3
Procedure
This compound was prepared from intermediate 247a and thionyl chloride according to the procedure used in Example 171. Received 3.53 g (75%).
Sources & evidence
- ORD record
- ord-69d2951e779243d7907f462affd15616
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06548494B1
Reaction notes
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