HCID 24729719, compound → HCID 76282246, compound
Reaction equation
[Cl:1][C:2]1[C:3]([O:11][CH2:12][CH:13]2[CH2:15][CH2:14]2)=[CH:4][C:5]([C:8]([OH:10])=O)=[N:6][CH:7]=1.[NH2:16][CH:17]([CH:21]1[CH2:23][CH2:22]1)[CH2:18][CH2:19][OH:20]>>[CH:21]1([CH:17]([NH:16][C:8]([C:5]2[CH:4]=[C:3]([O:11][CH2:12][CH:13]3[CH2:15][CH2:14]3)[C:2]([Cl:1])=[CH:7][N:6]=2)=[O:10])[CH2:18][CH2:19][OH:20])[CH2:23][CH2:22]1Participants
3
Procedure
The title compound was synthesized in analogy to Example 12d, using 5-chloro-4-cyclopropylmethoxy-pyridine-2-carboxylic acid and γ-amino-cyclopropanepropanol (CAN 683220-79-3) as starting materials and isolated (27 mg, 83%) as colorless oil; LC-MS (UV peak area, m/z) 97.6%, 325.1313 (MH+).
Workup
- customisolated (27 mg, 83%) as colorless oil
Sources & evidence
- ORD record
- ord-c8af8d7654c141a6beef7d17850a6adf
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09409866B2
Reaction notes
Loading…