Potassium Carbonate → HCID 22337389, compound
Reaction equation
C[O:2][C:3]([C:5]1[C:14]([CH3:15])=[C:13]2[C:8]([CH: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][CH: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 re action operation as in Starting Material Synthetic Example 6 using 4-(tert-butoxycarbonylamino)-8-methylthiochromane-7-carboxylic acid methyl ester (2.70 g) and potassium carbonate (4.42 g), the objective 4-(tert-butoxycarbonylamino)-8-methylthiochromane-7-carboxylic acid (1.80 g) was obtained as colorless crystals.
Sources & evidence
- ORD record
- ord-03bcdc87addd4dc69d60c5a31d9e23f2
- Source dataset
- uspto-grants-2005_08
- Patent number
- US06933305B2
Reaction notes
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