Formaldehyde → HCID 25030844, compound
Reaction equation
[CH:1]1([CH2:4][NH:5][C:6]2([CH2:9][O:10][C:11]3[CH:20]=[C:19]4[C:14]([C:15]([O:21][C:22]5[CH:23]=[C:24]6[C:29](=[CH:30][CH:31]=5)[C:28]([C:32]([NH:34][CH3:35])=[O:33])=[CH:27][CH:26]=[CH:25]6)=[CH:16][CH:17]=[N:18]4)=[CH:13][C:12]=3[O:36][CH3:37])[CH2:8][CH2:7]2)[CH2:3][CH2:2]1.C=O.[BH-](OC(C)=O)(OC(C)=O)O[C:42](C)=O.[Na+]>C(Cl)Cl>[CH:1]1([CH2:4][N:5]([CH3:42])[C:6]2([CH2:9][O:10][C:11]3[CH:20]=[C:19]4[C:14]([C:15]([O:21][C:22]5[CH:23]=[C:24]6[C:29](=[CH:30][CH:31]=5)[C:28]([C:32]([NH:34][CH3:35])=[O:33])=[CH:27][CH:26]=[CH:25]6)=[CH:16][CH:17]=[N:18]4)=[CH:13][C:12]=3[O:36][CH3:37])[CH2:7][CH2:8]2)[CH2:3][CH2:2]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound of Example 13 (40 mg) was mixed with HCHO (2 eq, 37% in H2O), NaBH(OAc)3 (2 eq) in DCM (5 ml) and stirred at RT for 3 hours. The reaction was evaporated and purified with silica gel column to give the titled product (20 mg). Mass: (M+1), 512
Workup
- customThe reaction was evaporated
- custompurified with silica gel column
Sources & evidence
- ORD record
- ord-3dd24e6a027d4f81b7ef9c79c30c35ac
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08513283B2
Reaction notes
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