Potassium Carbonate → HCID 59089460, compound
Reaction equation
C[O:2][C:3]([C:5]1[C:14]([CH3:15])=[C:13]2[C:8]([C@@H:9]([NH:16][C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])[CH2:10][CH2:11][S:12]2)=[CH:7][CH:6]=1)=[O:4].C(=O)([O-])[O-].[K+].[K+]>>[C:20]([O:19][C:17]([NH:16][C@@H:9]1[C:8]2[C:13](=[C:14]([CH3:15])[C:5]([C:3]([OH:4])=[O:2])=[CH:6][CH:7]=2)[S:12][CH2:11][CH2:10]1)=[O:18])([CH3:23])([CH3:22])[CH3:21]Participants
3
Procedure
By a similar reaction operation as in Starting Material Synthetic Example 6 using (S)-4-(tert-butoxycarbonylamino)-8-methylthiochromane-7-carboxylic acid methyl ester (5.00 g) and potassium carbonate (6.13 g), the objective (S)-4-(tert-butoxycarbonylamino)-8-methylthiochromane-7-carboxylic acid (4.06 g) was obtained as a colorless amorphous solid.
Sources & evidence
- ORD record
- ord-74852714f47d4013a5d70ac320fa7cd9
- Source dataset
- uspto-grants-2005_08
- Patent number
- US06933305B2
Reaction notes
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