1-Propanol, 3-amino-2,2-dimethyl- → HCID 10295552, compound
Reaction equation
[Cl:1][C:2]1[CH:21]=[CH:20][C:19]([CH:22]=O)=[CH:18][C:3]=1[C:4]([NH:6][CH2:7][C:8]12[CH2:17][CH:12]3[CH2:13][CH:14]([CH2:16][CH:10]([CH2:11]3)[CH2:9]1)[CH2:15]2)=[O:5].[NH2:24][CH2:25][C:26]([CH3:30])([CH3:29])[CH2:27][OH:28].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCCl>[Cl:1][C:2]1[CH:21]=[CH:20][C:19]([CH2:22][NH:24][CH2:25][C:26]([CH3:30])([CH3:29])[CH2:27][OH:28])=[CH:18][C:3]=1[C:4]([NH:6][CH2:7][C:8]12[CH2:17][CH:12]3[CH2:13][CH:14]([CH2:16][CH:10]([CH2:11]3)[CH2:9]1)[CH2:15]2)=[O:5]Participants
5
Procedure
Prepared according to the method described in Example 2 from 2-chloro-5-formyl-N-(tricyclo [3.3.1.13,7]dec-1-ylmethyl)-benzamide (0.150 g, Example 1b), 3-amino-2,2-dimethylpropanol (0.093 g) and sodium triacetoxyborohydride (0.134 g) in 1,2-dichloroethane (6 ml). After work-up, the residue was purified by NPHPLC eluting with a gradient of 0–10% ethanol in dichlorometane to give the title compound as a white powder (0.035 g).
Workup
- customPrepared
- customAfter work-up, the residue was purified by NPHPLC
- washeluting with a gradient of 0–10% ethanol in dichlorometane
Sources & evidence
- ORD record
- ord-31abcbb3a7944d39a6bb3968af62f096
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07132457B2
Reaction notes
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