Thionyl Chloride → HCID 69701630, compound
Reaction equation
[F:1][C:2]1[C:3]2[C:4]3[N:5]([C:13]([C:16]4[CH:21]=[CH:20][C:19]([CH2:22]O)=[CH:18][CH:17]=4)=[N:14][CH:15]=2)[CH2:6][CH2:7][C:8]=3[NH:9][C:10](=[O:12])[CH:11]=1.S(Cl)([Cl:26])=O.ClCC1C=CC(C2N3CCC4NC(=O)C=CC(C=43)=CN=2)=CC=1>>[Cl:26][CH2:22][C:19]1[CH:20]=[CH:21][C:16]([C:13]2[N:5]3[CH2:6][CH2:7][C:8]4[NH:9][C:10](=[O:12])[CH:11]=[C:2]([F:1])[C:3]([C:4]=43)=[CH:15][N:14]=2)=[CH:17][CH:18]=1Participants
4
Procedure
This compound was prepared from intermediate 97 and thionyl chloride using the procedure described in Example 171 for 171a. HPLC Rt=3.260 min.
Sources & evidence
- ORD record
- ord-74c5359b71ac453486d114d0ed61356a
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06548494B1
Reaction notes
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