2-Aminopropanol → HCID 68770956, compound

HRID 2194174Notes

Reaction equation

HRID 2194174 reaction equation
Cl[C:2]1[C:7]([S:8]([N:11]2[CH2:32][CH2:31][C:14]3([C:18](=[O:19])[N:17]([C:20]4[CH:25]=[CH:24][C:23]([O:26][C:27]([F:30])([F:29])[F:28])=[CH:22][CH:21]=4)[CH2:16][CH2:15]3)[CH2:13][CH2:12]2)(=[O:10])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[CH3:33][CH:34]([NH2:37])[CH2:35][OH:36]>>[OH:36][CH2:35][CH:34]([NH:37][C:2]1[C:7]([S:8]([N:11]2[CH2:32][CH2:31][C:14]3([C:18](=[O:19])[N:17]([C:20]4[CH:25]=[CH:24][C:23]([O:26][C:27]([F:28])([F:30])[F:29])=[CH:22][CH:21]=4)[CH2:16][CH2:15]3)[CH2:13][CH2:12]2)(=[O:9])=[O:10])=[CH:6][CH:5]=[CH:4][N:3]=1)[CH3:33]

Participants

3

Procedure

The title compound was prepared in analogy to example 189 from 8-(2-chloro-pyridine-3-sulfonyl)-2-(4-trifluoromethoxy-phenyl)-2,8-diaza-spiro[4.5]decan-1-one (described in example 188) and DL-2-amino-1-propanol. White solid. MS (ESI): 529.3 (MH+).

Sources & evidence

ORD record
ord-3d417bf6f16f4ac39a4b7825f1aff5aa
Source dataset
uspto-grants-2012_12
Patent number
US08329904B2

Reaction notes

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